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

STRYKER LAPAROSCOPE

K Number: K910132 · Decision Feb 21, 1991
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
124
Review Days
43

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Basic Information

Device Name
STRYKER LAPAROSCOPE
K Number
K910132
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Stryker Corp.
Date Received
January 9, 1991
Decision Date
February 21, 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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