Medical Device Manufacturer · US , Indianapolis , IN

Promedic, Inc. - FDA 510(k) Cleared Devices

16 submissions · 14 cleared · Since 1995

Recent clearances: EUM 100PRO, CLEARPATH 24, NON-IV ADAPTER FOR INFANT NG TUBE

View 16 510(k) Devices ↓

16

Total

14

Cleared

0

Denied

FDA 510(k) Regulatory Record - Promedic, Inc. Anesthesiology ✕

6 devices

1-6 of 6

Cleared Jul 11, 2006

Anesthesiology · 137d

Cleared Jun 21, 2006

Anesthesiology · 85d

Cleared Jan 28, 2003

GAS SAMPLING LINES

Anesthesiology · 96d

Cleared Jun 16, 1997

DATEX ENGSTOM MANUAL RESUSCITATOR

Anesthesiology · 89d

Cleared Jul 15, 1996

BURLEW INFANT HOOD

Anesthesiology · 39d

Cleared Jun 07, 1995

AIR-SOFT-DISPOSABLE, ANESTHESISA/RESPIRATORY FACE MASK

Anesthesiology · 92d