Medical Device Manufacturer · US , Irvine , CA

Telesair, Inc.

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied

Telesair, Inc. — FDA 510(k) Submissions

Telesair, Inc. has submitted 2 FDA 510(k) premarket notifications since 2023, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Humidifier, Respiratory Gas, (direct Patient Interface), Ventilator, Continuous, Facility Use . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Anesthesiology 2