FDA 510(k) Applications Submitted by MEDITEC CO., LTD.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K990380 |
02/08/1999 |
(1) DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-250; (2) FULLY AUTOMATIC BLOOD PRESSURE MONITOR, MODEL MD-700 |
MEDITEC CO., LTD. |
K002655 |
08/25/2000 |
DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-550 |
MEDITEC CO., LTD. |
K992328 |
07/12/1999 |
FUZZY AUTOMATIC BLOOD PRESSURE MONITOR MODELS MD-750, MD-770, MD-800 |
MEDITEC CO., LTD. |
K041789 |
07/02/2004 |
NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T |
MEDITEC CO., LTD. |
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