Hospitak, Inc.
United StatesFDA applicant, unverified
- Devices
- 27
What Hospitak, Inc. makes
Hospitak, Inc. manufactures single-use respiratory and oxygen delivery devices, including aerosol generators, nebulizers, anesthesia breathing circuits, manual resuscitators, mouthpieces, and incentive spirometers. The company also produces airway support items like inflatable air splints and pressure relief valves for oxygen cylinders, alongside adaptors and oxygen concentrators.
The portfolio comprises Class I and Class II medical devices, with submissions recorded under the FDA’s 510(k) clearance pathway. Products are listed in the U.S. regulatory registry, adhering to applicable FDA requirements for their respective risk classifications.
Catalogue
Search and filter all 27 devicesFrequently asked questions
How many devices does Hospitak, Inc. have in the registry?
The registry currently lists 27 devices for Hospitak, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hospitak, Inc.'s devices?
Among its 27 most recently registered devices, Hospitak, Inc. has devices listed in FDA 510(k) (27 devices).
What risk classes do Hospitak, Inc.'s devices fall under?
Among its 27 most recently registered devices, the classes recorded for Hospitak, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hospitak, Inc. in the registry?
The most recently registered devices listed for Hospitak, Inc. include DISPOSABLE AEROSOL T, DISPOSABLE MEDICATION NEBULIZER, BREATHING CIRCUIT PRODUCTS, ANESTHESIA and DISPOSABLE, MANUAL PULMONARY RESUSCITATOR.