FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

UROSURGE ACUTRAINER

K Number: K962770 · Decision Aug 1, 1996
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
36
Applicant Total
4
Review Days
16

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Basic Information

Device Name
UROSURGE ACUTRAINER
K Number
K962770
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.2040
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Princeton Regulatory Assoc.
Date Received
July 16, 1996
Decision Date
August 1, 1996
Product Code
KPN
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KPN Alarm, Conditioned Response Enuresis

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KPN), ordered by most recent decision date.

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Other Clearances by Princeton Regulatory Assoc.

K Number Device Name
K965136 UROSURGE UROTHERM FLUID WARMING SYSTEM
K972158 GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES
K973504 UROSURGE UROSTENT