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

LOOP RETRIEVER

K Number: K830802 · Decision Apr 28, 1983
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
73
Applicant Total
52
Review Days
45

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Basic Information

Device Name
LOOP RETRIEVER
K Number
K830802
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Van-Tec, Inc.
Date Received
March 14, 1983
Decision Date
April 28, 1983
Product Code
OCZ
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
OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered

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