Medical Device Manufacturer · US , Columbia , MD

Meridian Medical Technologies, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997

Recent clearances: PRIME ECG SYSTEM, PRIME ECG SYSTEM, CARDIOBEEPER CB-12L

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Meridian Medical Technologies, Inc. Cardiovascular ✕

3 devices

1-3 of 3

Cleared Jun 11, 2003

PRIME ECG SYSTEM

Cardiovascular · 149d

Cleared Mar 06, 2002

PRIME ECG SYSTEM

Cardiovascular · 219d

Cleared Mar 17, 1997

CARDIOBEEPER CB-12L

Cardiovascular · 87d