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

BARIATRIC LAPAROSCOPE, MODEL 367

K Number: K993045 · Decision Oct 27, 1999
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
101
Review Days
47

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Basic Information

Device Name
BARIATRIC LAPAROSCOPE, MODEL 367
K Number
K993045
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
September 10, 1999
Decision Date
October 27, 1999
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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