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

ULTRA-VIOLET GLUCOSE REAGENT

K Number: K851514 · Decision May 20, 1985
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
1
Applicant Total
19
Review Days
35

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Basic Information

Device Name
ULTRA-VIOLET GLUCOSE REAGENT
K Number
K851514
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bio-Analytics Laboratories, Inc.
Date Received
April 15, 1985
Decision Date
May 20, 1985
Product Code
CFA
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
CFA Electrode, Ion Specific, Magnesium

Similar 510(k) Clearances

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Other Clearances by Bio-Analytics Laboratories, Inc.

K Number Device Name
K861638 KINETIC ALKALINE PHOSPHATASE REAGENT KIT
K860245 ENZYMATIC ALPHA-AMYLASE REAGENT KIT
K860213 ALBUMIN REAGENT KIT
K851513 ULTRA-VIOLET BUN REAGENT KIT
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. →