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

OLYMPUS IGA IMMUNOTURBIDIMETRIC REAGENT

K Number: K951055 · Decision Apr 17, 1995
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
11
Applicant Total
149
Review Days
41

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Basic Information

Device Name
OLYMPUS IGA IMMUNOTURBIDIMETRIC REAGENT
K Number
K951055
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Olympus America, Inc.
Date Received
March 7, 1995
Decision Date
April 17, 1995
Product Code
CFQ
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
CFQ Radioimmunoassay, Immunoglobulins (G, A, M)

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K Number Device Name
K111788 ENDOEYE HD II
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K073487 OLYMPUS IGM REAGENT
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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