Iquum, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Liat Strep A Assay Ref K141338
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iquum, Inc. have in the registry?
The registry currently lists 3 devices for Iquum, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iquum, Inc.'s devices?
Among its 3 most recently registered devices, Iquum, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Iquum, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Iquum, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iquum, Inc. in the registry?
The most recently registered devices listed for Iquum, Inc. include LIAT STREP A ASSAY, LIAT (TM) INFLUENZA A / B ASSAY, LIAT (TM) ANALYZER and cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System.