FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OLYMPUS INORGANIC PHOSPHORUS REAGENT

K Number: K944768 · Decision Mar 24, 1995
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
149
Review Days
178

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Basic Information

Device Name
OLYMPUS INORGANIC PHOSPHORUS REAGENT
K Number
K944768
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Olympus America, Inc.
Date Received
September 27, 1994
Decision Date
March 24, 1995
Product Code
CEO
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

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K Number Device Name
K111788 ENDOEYE HD II
K081615 OLYMPUS CEA - CARCINOEMBRYONIC ANTIGEN
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
Search all 149 clearances from Olympus America, Inc. →