Viva-Tek Assoc., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Viva-Tek Assoc., Inc. makes
Viva-Tek Associates, Inc. manufactures the AIRES, a respiratory therapy device designed for airway clearance, and the GO-CLEAN, a portable suction system for clinical use.
The company’s products are regulated as Class II medical devices in the U.S. and are listed under FDA’s 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Frequently asked questions
How many devices does Viva-Tek Assoc., Inc. have in the registry?
The registry currently lists 2 devices for Viva-Tek Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viva-Tek Assoc., Inc.'s devices?
Among its 2 most recently registered devices, Viva-Tek Assoc., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Viva-Tek Assoc., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Viva-Tek Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Viva-Tek Assoc., Inc. in the registry?
The most recently registered devices listed for Viva-Tek Assoc., Inc. include AIRES and GO-CLEAN.