New England Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What New England Medical, Inc. makes
New England Medical, Inc. manufactures grounding pads, which are adhesive electrodes used in medical procedures to safely conduct electrical currents during electrotherapy or defibrillation.
The company’s grounding pads are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The products are intended for use in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
New England Medical Grounding Pad Ref K931982
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New England Medical, Inc. have in the registry?
The registry currently lists 2 devices for New England Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list New England Medical, Inc.'s devices?
Among its 2 most recently registered devices, New England Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do New England Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for New England Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from New England Medical, Inc. in the registry?
The most recently registered devices listed for New England Medical, Inc. include TRUCONE ROTATIONAL CONE BIOPSY INSTRUMENT, MODEL 231812 - 233018 and NEW ENGLAND MEDICAL GROUNDING PAD.