Princeton Regulatory Assoc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Princeton Regulatory Assoc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Princeton Regulatory Assoc. has 4 FDA 510(k) cleared medical devices. Based in Princeton, US.
Historical record: 4 cleared submissions from 1996 to 1998. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Princeton Regulatory Assoc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Princeton Regulatory Assoc.
4 devices
Cleared
Oct 16, 1998
UROSURGE UROTHERM FLUID WARMING SYSTEM
General Hospital
662d
Cleared
Feb 20, 1998
GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES
General Hospital
256d
Cleared
Jan 30, 1998
UROSURGE UROSTENT
Gastroenterology & Urology
136d
Cleared
Aug 01, 1996
UROSURGE ACUTRAINER
Gastroenterology & Urology
16d