Novabay Pharmaceuticals, Inc. is one of 13028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novabay Pharmaceuticals, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iCase Contact Lens Case, NEUTROPHASE(R) SKIN AND WOUND CLEANSER OTC
2
Total
2
Cleared
0
Denied
Novabay Pharmaceuticals, Inc. has 2 FDA 510(k) cleared medical devices. Based in Chevy Chase, US.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Novabay Pharmaceuticals, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Foresight Regulatory Strategies, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Novabay Pharmaceuticals, Inc.
2 devices