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

KINETIC ALKALINE PHOSPHATASE REAGENT KIT

K Number: K861638 · Decision May 29, 1986
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
123
Applicant Total
19
Review Days
29

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Basic Information

Device Name
KINETIC ALKALINE PHOSPHATASE REAGENT KIT
K Number
K861638
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bio-Analytics Laboratories, Inc.
Date Received
April 30, 1986
Decision Date
May 29, 1986
Product Code
CJE
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
CJE Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes

Similar 510(k) Clearances

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Other Clearances by Bio-Analytics Laboratories, Inc.

K Number Device Name
K860245 ENZYMATIC ALPHA-AMYLASE REAGENT KIT
K860213 ALBUMIN REAGENT KIT
K851513 ULTRA-VIOLET BUN REAGENT KIT
K851514 ULTRA-VIOLET GLUCOSE REAGENT
K850639 ENZYMATIC ALPHA-AMYLASE REAGENT KIT
K832771 ERYTHROCYTE TEST
K832567 ACETAMINOPHEN(PARACETAMOL
K831414 COLORIMETRIC BUN
K821934 BIO-CAL OPERATION CHECK KIT
K813431 SALICYLATES
Search all 19 clearances from Bio-Analytics Laboratories, Inc. →