Prytime Medical Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: pREBOA-PRO Catheter, pREBOA-PRO Catheter, ER-REBOA PLUS Catheter
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Prytime Medical Devices, Inc. Cardiovascular ✕
5 devices
Cleared
CT
Sep 05, 2025
pREBOA-PRO Catheter
Cardiovascular
269d
Cleared
Jun 03, 2020
pREBOA-PRO Catheter
Cardiovascular
99d
Cleared
Jan 09, 2020
ER-REBOA PLUS Catheter
Cardiovascular
29d
Cleared
Nov 08, 2017
ER-REBOA Catheter
Cardiovascular
54d
Cleared
Apr 04, 2017
ER-REBOA Catheter
Cardiovascular
53d