Emed, Inc.
Also registered as E-Med Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Emed, Inc. makes
Emed, Inc. makes the FLASH 1 device.
The FLASH 1 is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Site Strip Ref K843200
Regimes: 510(k) Registry: 510(k)I.V. Strip Ref K792049
Regimes: 510(k) Registry: 510(k)Microfuse Membrane Infusion Catheter Ref K971619
Regimes: 510(k) Registry: 510(k)Flash 1 Ref K022583
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emed, Inc. have in the registry?
The registry currently lists 4 devices for Emed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emed, Inc.'s devices?
Among its 4 most recently registered devices, Emed, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Emed, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Emed, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emed, Inc. in the registry?
The most recently registered devices listed for Emed, Inc. include SITE STRIP, I.V. STRIP, MICROFUSE MEMBRANE INFUSION CATHETER and FLASH 1.