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

RAICHEM(TM) MAGNESIUM REAGENT, ENZYMATIC

K Number: K880880 · Decision May 27, 1988
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
63
Review Days
86

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Basic Information

Device Name
RAICHEM(TM) MAGNESIUM REAGENT, ENZYMATIC
K Number
K880880
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Reagents Applications, Inc.
Date Received
March 2, 1988
Decision Date
May 27, 1988
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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K915191 RAI-TROL ELEVATED LIPIDS CONTROL
K913398 RAICHEM(TM) CREATINE KINASE-MB REAGENT
K911900 RAICHEM SPIA C3 REAGENT
K911899 RAICHEM SPIA C4 REAGENT
K911898 RAICHEM(TM) SPIA(TM) HAPTOGLOBIN REAGENT
K905084 RAICHEM CREATINE KINASE REAGENT, OPTIMIZED UV
K905085 RAICHEM GGT REAGENT
Search all 63 clearances from Reagents Applications, Inc. →