Medical Device Manufacturer · US , Houston , TX

Preemicare Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1988

9

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Preemicare Corp. General Hospital ✕

5 devices

1-5 of 5

Cleared May 02, 1990

MODEL 130 AUTOMATIC HEIGHT ADJUST (AHA) INCUBATOR

General Hospital · 75d

Cleared Sep 27, 1989

PREEMICARE MODEL 2500 TRANSPORT WARMER

General Hospital · 139d

Cleared Aug 07, 1989

PREEMICARE SERIES 2000 INFANT WARMER

General Hospital · 222d

Cleared Mar 08, 1989

PREEMICARE SERIES 4000 PHOTOTHERAPY LAMP

General Hospital · 159d

Cleared Dec 08, 1988

PREEMICARE MODEL D1-X1, SERIES 3000

General Hospital · 245d