Proact, Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Proact, Ltd. Gastroenterology & Urology ✕
4 devices
Cleared
Jul 13, 1994
QUICK CORE II
Gastroenterology & Urology
121d
Cleared
Mar 22, 1993
PROACT BIOPSY NEEDLE ENCHANCEMENTS
Gastroenterology & Urology
81d
Cleared
Oct 01, 1990
BAUER FLEXI-TEMNO BIOPSY NEEDLE
Gastroenterology & Urology
131d
Cleared
Sep 06, 1990
BAUER TEMNO BIOPSY NEEDLE
Gastroenterology & Urology
106d