Bill Olson Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Bill Olson Corp. makes
Bill Olson Corp. manufactures anesthesia breathing circuit kits and circuits for both adult and pediatric patients. Their product line also includes bacterial and viral filters designed for use with these breathing circuits.
The company is based in the United States and maintains a portfolio consisting of Class I and Class II medical devices. These products are listed within the FDA 510(k) regulatory registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Zefon Baterial/Viral Filter Ref K911651
Regimes: 510(k) Registry: 510(k)Zefon Adult Anesthesia Breathing Circuit Ref K911880
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bill Olson Corp. have in the registry?
The registry currently lists 4 devices for Bill Olson Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bill Olson Corp.'s devices?
Among its 4 most recently registered devices, Bill Olson Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Bill Olson Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Bill Olson Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bill Olson Corp. in the registry?
The most recently registered devices listed for Bill Olson Corp. include ZEFON PEDIATRIC ANESTHESIA BREATHING CIRCUIT KITS, ZEFON ADULT ANESTHESIA BREATHING CIRCUIT WITH FILTER, ZEFON PEDIATRIC ANESTHESIA BREATHING CIRCUIT WITH FILTER, ZEFON BATERIAL/VIRAL FILTER and ZEFON ADULT ANESTHESIA BREATHING CIRCUIT.