Oemedic International, Inc. is one of 25737 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oemedic International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OEMEDIC INTERNATIONAL INC. BESMED SILICONE ADULT, CHILD, INFANT MANUAL RESUSCITATOR WITH MASK AND RESERVOIR, OEMEDIC INTERNATIONAL INC. BESMED SINGLE USE ADULT, CHILD, INFANT MANUAL RESUSCITATOR WITH MASK & RESERVOIR
2
Total
2
Cleared
0
Denied
Oemedic International, Inc. has 2 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 2 cleared submissions from 2002 to 2002. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Oemedic International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oemedic International, Inc.
2 devices