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

FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER

K Number: K944790 · Decision Nov 29, 1994
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
23
Applicant Total
58
Review Days
62

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Basic Information

Device Name
FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
K Number
K944790
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Applied Medical Resources
Date Received
September 28, 1994
Decision Date
November 29, 1994
Product Code
GBZ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GBZ Catheter, Cholangiography

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