Medical Device Manufacturer · IE , Belfast

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

3 submissions · 3 cleared · Since 2000
3
Total
3
Cleared
0
Denied

Meridian Medical Technologies , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Belfast, IE.

Historical record: 3 cleared submissions from 2000 to 2001. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Meridian Medical Technologies , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Meridian Medical Technologies , Ltd.

3 devices
1-3 of 3
Cleared Oct 23, 2001
TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII
K011058 · DXN
Cardiovascular · 200d
Cleared May 10, 2001
BRIDGE III RECEIVER
K010794 · DXH
Cardiovascular · 55d
Cleared Oct 25, 2000
CARDIOBEEPER CB12/12, MODEL CB12/12
K002310 · DXH
Cardiovascular · 86d
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All3 Cardiovascular 3