Emergency Filtration Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Emergency Filtration Products, Inc. makes
Emergency Filtration Products, Inc. manufactures medical-grade respiratory filters, including the RESPAIDE filter and breathing circuit filters designed to improve air quality in critical care and emergency ventilation systems.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Respaide Ref K980052
Regimes: 510(k) Registry: 510(k)Breathing Circuit Filter Ref K012958
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emergency Filtration Products, Inc. have in the registry?
The registry currently lists 2 devices for Emergency Filtration Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emergency Filtration Products, Inc.'s devices?
Among its 2 most recently registered devices, Emergency Filtration Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Emergency Filtration Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Emergency Filtration Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emergency Filtration Products, Inc. in the registry?
The most recently registered devices listed for Emergency Filtration Products, Inc. include RESPAIDE and BREATHING CIRCUIT FILTER.