Applied Technology Ventures, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Applied Technology Ventures, LLC makes
Applied Technology Ventures, LLC manufactures Class II medical devices for drug screening, including a handheld fingerprint drug screening device and a Genie Cup integrated screening system designed for rapid on-site testing.
The company’s portfolio is regulated under the FDA’s 510(k) pathway as Class II devices and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Fingerprint Drug Screening Device Ref K973726
Regimes: 510(k) Registry: 510(k)Genie Cup Integrated Screening Device Ref K980836
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Applied Technology Ventures, LLC have in the registry?
The registry currently lists 2 devices for Applied Technology Ventures, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Applied Technology Ventures, LLC's devices?
Among its 2 most recently registered devices, Applied Technology Ventures, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Applied Technology Ventures, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Applied Technology Ventures, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Applied Technology Ventures, LLC in the registry?
The most recently registered devices listed for Applied Technology Ventures, LLC include FINGERPRINT DRUG SCREENING DEVICE and GENIE CUP INTEGRATED SCREENING DEVICE.