International Respiratory Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What International Respiratory Systems, Inc. makes
International Respiratory Systems, Inc. manufactures manual resuscitators, manual pulmonary resuscitators with rubber compression bags, and PEEP valves.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Peep Valve Ref K923618
Regimes: 510(k) Registry: 510(k)International Respiratory Systems, Inc.'s Manual Pulmonary Resuscitator With Rubber Compression Bag Ref K981308
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does International Respiratory Systems, Inc. have in the registry?
The registry currently lists 3 devices for International Respiratory Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list International Respiratory Systems, Inc.'s devices?
Among its 3 most recently registered devices, International Respiratory Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do International Respiratory Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for International Respiratory Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from International Respiratory Systems, Inc. in the registry?
The most recently registered devices listed for International Respiratory Systems, Inc. include INTERNATIONAL RESPIRATORY SYSTEMS, INC.'S MANUAL RESUSCIATOR, PEEP VALVE and INTERNATIONAL RESPIRATORY SYSTEMS, INC.'S MANUAL PULMONARY RESUSCITATOR WITH RUBBER COMPRESSION BAG.