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

OLYMPUS MAGNESIUM REAGENT

K Number: K944407 · Decision Dec 27, 1994
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
149
Review Days
110

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Basic Information

Device Name
OLYMPUS MAGNESIUM REAGENT
K Number
K944407
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Olympus America, Inc.
Date Received
September 8, 1994
Decision Date
December 27, 1994
Product Code
JGJ
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
JGJ Photometric Method, Magnesium

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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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