Medical Device Manufacturer · US , Fort Myers , FL

Intertech Resources, Inc. - FDA 510(k) Cleared Devices

29 submissions · 27 cleared · Since 1987

29

Total

27

Cleared

0

Denied

FDA 510(k) Regulatory Record - Intertech Resources, Inc. General Hospital ✕

3 devices

1-3 of 3

Cleared Jun 08, 1995

General Hospital · 37d

Cleared Jul 01, 1993

HEPA FILTERED HME

General Hospital · 134d

Cleared Sep 30, 1988

RESUSCITATION BAG EXHALATION FILTER

General Hospital · 32d