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

CATHETER, SAMPLING, CONDUIT

K Number: K771066 · Decision Jul 11, 1977
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
0
Applicant Total
61
Review Days
28

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Basic Information

Device Name
CATHETER, SAMPLING, CONDUIT
K Number
K771066
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Mentor Corp.
Date Received
June 13, 1977
Decision Date
July 11, 1977
Product Code
FEZ
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
FEZ Catheter And Tube, Suprapubic

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K031767 MENTOR OBTAPE TRANS-OBTURATOR TAPE
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