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

FLEXIBLE BIOPSY FORCEP

K Number: K871809 · Decision Jun 18, 1987
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
73
Applicant Total
1
Review Days
41

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Basic Information

Device Name
FLEXIBLE BIOPSY FORCEP
K Number
K871809
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Surgi-Aid Endoscopics, Inc.
Date Received
May 8, 1987
Decision Date
June 18, 1987
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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