FDA 510(k) Applications Submitted by PRINCETON REGULATORY ASSOC.

FDA 510(k) Number Submission Date Device Name Applicant
K972158 06/09/1997 GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES PRINCETON REGULATORY ASSOC.
K962770 07/16/1996 UROSURGE ACUTRAINER PRINCETON REGULATORY ASSOC.
K973504 09/16/1997 UROSURGE UROSTENT PRINCETON REGULATORY ASSOC.
K965136 12/23/1996 UROSURGE UROTHERM FLUID WARMING SYSTEM PRINCETON REGULATORY ASSOC.


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