FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VAS DILATOR

K Number: K922192 · Decision Aug 7, 1992
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
43
Applicant Total
104
Review Days
88

Basic Information

Device Name
VAS DILATOR
K Number
K922192
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
COOK UROLOGICAL, INC.
Date Received
May 11, 1992
Decision Date
August 7, 1992
Product Code
KOA
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
KOA Surgical Instruments, G-U, Manual (And Accessories)

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