Hall Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pristine Specimen Tube And Introducer System Ref K881514
Regimes: 510(k) Registry: 510(k)Closed Wound Drainage Systems Ref K874645
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hall Laboratories, Inc. have in the registry?
The registry currently lists 2 devices for Hall Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hall Laboratories, Inc.'s devices?
Among its 2 most recently registered devices, Hall Laboratories, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hall Laboratories, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hall Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hall Laboratories, Inc. in the registry?
The most recently registered devices listed for Hall Laboratories, Inc. include PRISTINE SPECIMEN TUBE AND INTRODUCER SYSTEM and CLOSED WOUND DRAINAGE SYSTEMS.