FDA 510(k) Applications Submitted by MERIDIAN MEDICAL TECHNOLOGIES LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K002310 | 07/31/2000 | CARDIOBEEPER CB12/12, MODEL CB12/12 | MERIDIAN MEDICAL TECHNOLOGIES LTD. |
| K010794 | 03/16/2001 | BRIDGE III RECEIVER | MERIDIAN MEDICAL TECHNOLOGIES LTD. |
| K011058 | 04/06/2001 | TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII | MERIDIAN MEDICAL TECHNOLOGIES LTD. |
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