Meditec Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Meditec Co., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Meditec Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Sunnamcity, Kyunggido, KR.
Historical record: 4 cleared submissions from 1999 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Meditec Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meditec Co., Ltd.
4 devices
Cleared
Jul 15, 2004
NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T
Cardiovascular
13d
Cleared
Sep 06, 2000
DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-550
Cardiovascular
12d
Cleared
Jul 21, 1999
FUZZY AUTOMATIC BLOOD PRESSURE MONITOR MODELS MD-750, MD-770, MD-800
Cardiovascular
9d
Cleared
Feb 22, 1999
(1) DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-250
Cardiovascular
14d