Pryor Medical Devices, Inc. is one of 18431 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pryor Medical Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ER-REBOA Catheter
1
Total
1
Cleared
0
Denied
Pryor Medical Devices, Inc. has 1 FDA 510(k) cleared medical devices. Based in Boeme, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pryor Medical Devices, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by CardioMed Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pryor Medical Devices, Inc.
1 devices