Leigh Med Tech, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Leigh Med. Tech. Laryngoscope Blade Cover Ref K951147
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Leigh Med Tech, Inc. have in the registry?
The registry currently lists 2 devices for Leigh Med Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Leigh Med Tech, Inc.'s devices?
Among its 2 most recently registered devices, Leigh Med Tech, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Leigh Med Tech, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Leigh Med Tech, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Leigh Med Tech, Inc. in the registry?
The most recently registered devices listed for Leigh Med Tech, Inc. include AUTOMATED DISPOSABLE SOFT TISSUE BIOPSY ASPIR. DEV and LEIGH MED. TECH. LARYNGOSCOPE BLADE COVER.