Voguestrap is one of 21656 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Voguestrap - FDA 510(k) Cleared Devices
Recent clearances: IMAG, IPOD, EZ-FIND AND ISLIDE
1
Total
1
Cleared
0
Denied
Voguestrap has 1 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Voguestrap Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Voguestrap
1 devices