Meditec Co., Ltd. is one of 419 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
Recent clearances: NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T, FUZZY AUTOMATIC BLOOD PRESSURE MONITOR MODELS MD-750, MD-770, MD-800, (1) DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-250
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.
Regulatory submissions have been managed by Tuv Product Service, Inc. and Underwriters Laboratories, Inc..
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