Collectovac, Inc.
Country not established
- Devices
- 1
What Collectovac, Inc. makes
Collectovac, Inc. manufactures The Blue Mask, a respiratory device designed for use in medical settings to deliver oxygen or other inhaled therapies to patients. The product is intended for applications requiring controlled airflow and is primarily used in clinical environments.
The company’s portfolio is regulated under Class I medical devices in the United States, with The Blue Mask authorised via the FDA’s 510(k) clearance process. The device is listed in the FDA’s regulatory database under this classification.
Catalogue
The Blue Mask Ref K782163
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Collectovac, Inc. have in the registry?
The registry currently lists 1 device for Collectovac, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Collectovac, Inc.'s devices?
Among its 1 most recently registered device, Collectovac, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Collectovac, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Collectovac, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Collectovac, Inc. in the registry?
The most recently registered devices listed for Collectovac, Inc. include THE BLUE MASK.