Lamtic, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Accu-Drop I.V. Extension Set Ref K923560
Regimes: 510(k) Registry: 510(k)Ac-901 I.V. Infusion Drop Counter Ref K923561
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lamtic, Inc. have in the registry?
The registry currently lists 2 devices for Lamtic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lamtic, Inc.'s devices?
Among its 2 most recently registered devices, Lamtic, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lamtic, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lamtic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lamtic, Inc. in the registry?
The most recently registered devices listed for Lamtic, Inc. include ACCU-DROP I.V. EXTENSION SET and AC-901 I.V. INFUSION DROP COUNTER.