Wicab, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
2
Total
1
Cleared
1
Denied
Wicab, Inc. has 1 FDA 510(k) cleared medical devices. Based in Philedelphia, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Wicab, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Wicab, Inc.
2 devices