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

OES LAPARO-THORACO VIDEOSCOPE (RIGID)

K Number: K955456 · Decision Feb 22, 1996
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
336
Applicant Total
145
Review Days
85

Basic Information

Device Name
OES LAPARO-THORACO VIDEOSCOPE (RIGID)
K Number
K955456
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OLYMPUS AMERICA, INC.
Date Received
November 29, 1995
Decision Date
February 22, 1996
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

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