Pryon Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Pryon Corp. makes
Pryon Corp. manufactures airway management devices, including the CAP 400 AT, a reusable airway adapter, and the A-200 Multi-Use Airway Adapter. Their portfolio also includes capnography and pulse oximetry solutions, such as the P-300 Capnograph and Pulse Oximeter, as well as low dead space and reusable airway adaptors designed for respiratory monitoring and patient ventilation.
These devices are classified under Class II in the US and are listed via FDA 510(k) clearance. Pryon Corp. is based in the United States.
Catalogue
Cap 400 At Ref K935272
Regimes: 510(k) Registry: 510(k)A-200 Multi-Use Airway Adapter Ref K942772
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
P-300 Capnograph And Pulse Oximeter Ref K915773
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pryon Corp. have in the registry?
The registry currently lists 4 devices for Pryon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pryon Corp.'s devices?
Among its 4 most recently registered devices, Pryon Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Pryon Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Pryon Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pryon Corp. in the registry?
The most recently registered devices listed for Pryon Corp. include CAP 400 AT, A-200 MULTI-USE AIRWAY ADAPTER, LOW DEAD SPACE ADAPTOR & REUASABLE AIRWAY ADAPTOR and P-300 CAPNOGRAPH AND PULSE OXIMETER.