Biowatch Medical, Inc. is one of 24119 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Biowatch Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Columbia, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Biowatch Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biowatch Medical, Inc.
1 devices