Osi Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
Osi Medical Dolphin Stand-Alone Pulse Oximeter & Digital Dolphin Disposable Optical Sendor Ref K012626
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osi Medical, Inc. have in the registry?
The registry currently lists 3 devices for Osi Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osi Medical, Inc.'s devices?
Among its 3 most recently registered devices, Osi Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Osi Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Osi Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osi Medical, Inc. in the registry?
The most recently registered devices listed for Osi Medical, Inc. include OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER & DIGITAL DOLPHIN DISPOSABLE OPTICAL SENDOR, MODIFICATION TO OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER AND ACCESSORIES and OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER, MODEL 2100 AND DIGITAL DOLPHIN OPTICAL SENSOR, CLIP-ON FINGER PROBE, MOD.