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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