OKW has extended its unique Art-Case range of plastic electronic enclosures. Due to customer demand, four new rectangular models have been added, in addition to the existing round and oval versions.
Nutec Components, Inc., a leading manufacturer of advanced precision motion systems, offers a newly upgraded version of its T-MAX 5 low profile direct drive rotary servo positioning stage, enabling the device to deliver higher load capacity and improved trajectory control.
TechMESH Knitted Wire gaskets from Leader Tech make reliable electrical contact between parallel metallic surfaces in broad ranging electronic enclosures.
This innovative connector provides a single, fast, and reliable multi-way connection that offers extensive time savings when compared to traditional connections between individual pipes.
Medical device maker St. Jude Medical Inc. said Thursday it received Japanese regulatory approval for its Therapy Cool Patch Ablation Catheter, aimed treating irregular heartbeats.Shares of St. Jude rose 11 cents to $36.50 in morning trading Thursday.
(Cedars-Sinai Medical Center) The nerve cell-damaging plaque that builds up in the brain with Alzheimer's disease also builds up in the retinas of the eyes -- and it shows up there earlier, leading to the prospect that noninvasive optical imaging of the eyes could lead to earlier...
PressurexÂ® sensor film needed to measure contact pressure variations across flip chip dies and bonding tools.
Boston Scientific Announces FDA Approval and Launch of Lead Splitters for the Precision Plusâ„¢ Spinal Cord Stimulator SystemJune 24, 2010 6:37 am | by Boston Scientific | News | Comments
Two new splitters allow multi-site placement of up to four spinal cord stimulation leads
By Jeff Shuren, M.D., J.D., Director of FDA's Center for Devices and Radiological Health.
Federal Register: Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval ApplicationsJune 24, 2010 6:32 am | by U.S. Food & Drug Administration | News | Comments
This list is intended to inform the public of the availability of safety and effectiveness summaries of approved PMAs through the Internet and the agency's Division of Dockets Management.
Federal Register: General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee; Notice of MeetingJune 24, 2010 6:31 am | by U.S. Food & Drug Administration | News | Comments
On August 26, 2010, the committee will discuss, make recommendations, and vote on premarket approval application for MelaFind, sponsored by MELA Sciences, Inc. MelaFind is a non-invasive computer vision system intended to assist in the evaluation of...
The ability to communicate is an elementary part of our lives, and without good hearing, communication becomes difficult if not impossible. This is why researchers continue to work on optimizing prostheses that improve hearing. Now researchers at the Universität Stuttgart in Germany have opened up a new avenue of
(American Thoracic Society) Exposure to high levels of fungus may increase the risk of severe asthma attacks among people with certain chitinase gene variants, according to a study from Harvard Medical School, Harvard Pilgrim Health Care Institute and Brigham and Women's Hospital.
Mersana Therapeutics Inc. has begun a Phase 1 trial of its anti-cancer drug candidate, designed to assess its safety and absorption in the body for patients with advanced solid tumors.
There are big savings in time and money for biotechs and pharmaceutical companies that turn to cloud computing, but it may only be for a while, not necessarily for the long term.