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

OLYMPUS BASKET GRASPERS

K Number: K955063 · Decision Jan 22, 1996
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
73
Applicant Total
149
Review Days
77

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Basic Information

Device Name
OLYMPUS BASKET GRASPERS
K Number
K955063
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Olympus America, Inc.
Date Received
November 6, 1995
Decision Date
January 22, 1996
Product Code
OCZ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered

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K073490 OLYMPUS IGG REAGENT
K073489 OLYMPUS IGA REAGENT
K062862 OLYMPUS URIC ACID REAGENT, MODEL OSR6X98
K063804 OLYMPUS TRIGLYCERIDE TEST SYSTEM
K061499 OSFERION
K062581 OLYMPUS TSH REAGENT, CALIBRATOR AND CONTROL AND AU3000I IMMUNOASSAY SYSTEM
K061575 OLYMPUS CALCIUM ARSENAZO REAGENT, OSR60117, OSR61117, OSR65117
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