Osi Medical, Inc. is one of 25737 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osi Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER & DIGITAL DOLPHIN DISPOSABLE OPTICAL SENDOR, MODIFICATION TO OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER AND ACCESSORIES, OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER, MODEL 2100 AND DIGITAL DOLPHIN OPTICAL SENSOR, CLIP-ON FINGER PROBE, MOD
3
Total
3
Cleared
0
Denied
Osi Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 3 cleared submissions from 2001 to 2001. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Osi Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Osi Medical, Inc.
3 devices
Cleared
Nov 02, 2001
OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER & DIGITAL DOLPHIN DISPOSABLE...
Anesthesiology
81d
Cleared
Aug 22, 2001
MODIFICATION TO OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER AND ACCESSORIES
Anesthesiology
16d
Cleared
Apr 17, 2001
OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER, MODEL 2100 AND DIGITAL...
Anesthesiology
286d