Wenzhou Bokang Instrument Co.,Ltd is one of 25373 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wenzhou Bokang Instrument Co.,Ltd - FDA 510(k) Cleared Devices
Recent clearances: ANEROID SPHYGMOMANOMETER, MODEL BK2002
1
Total
1
Cleared
0
Denied
Wenzhou Bokang Instrument Co.,Ltd has 1 FDA 510(k) cleared medical devices. Based in Metairie, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Wenzhou Bokang Instrument Co.,Ltd Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Center For Measurement Standards of Industrial as regulatory consultant.
FDA 510(k) Regulatory Record - Wenzhou Bokang Instrument Co.,Ltd
1 devices