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

CANNULA AND TROCAR

K Number: K912836 · Decision Aug 28, 1991
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
1
Review Days
63

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Basic Information

Device Name
CANNULA AND TROCAR
K Number
K912836
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Oceanside Biomedics
Date Received
June 26, 1991
Decision Date
August 28, 1991
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
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
GCJ Laparoscope, General & Plastic Surgery

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