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

HD ENDOEYE LAPARO-THORACO VIDEOSCOPE OLYMPUS LTF TYPE VH

K Number: K080948 · Decision Sep 26, 2008
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
81
Review Days
176

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Basic Information

Device Name
HD ENDOEYE LAPARO-THORACO VIDEOSCOPE OLYMPUS LTF TYPE VH
K Number
K080948
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 Medical Systems Corporation
Date Received
April 3, 2008
Decision Date
September 26, 2008
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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