Perrigo New York, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Perrigo New York, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Personal Lubricating Jelly
1
Total
1
Cleared
0
Denied
Perrigo New York, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bronx, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Perrigo New York, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Phil Triolo and Associates LC as regulatory consultant.
FDA 510(k) Regulatory Record - Perrigo New York, Inc.
1 devices