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

ERYTHROCYTE TEST

K Number: K832771 · Decision Oct 28, 1983
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
1
Applicant Total
19
Review Days
73

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Basic Information

Device Name
ERYTHROCYTE TEST
K Number
K832771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7100
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Bio-Analytics Laboratories, Inc.
Date Received
August 16, 1983
Decision Date
October 28, 1983
Product Code
LKZ
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
LKZ Red-Cell Count By Photometry

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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
K851514 ULTRA-VIOLET GLUCOSE REAGENT
K850639 ENZYMATIC ALPHA-AMYLASE REAGENT KIT
K832567 ACETAMINOPHEN(PARACETAMOL
K831414 COLORIMETRIC BUN
K821934 BIO-CAL OPERATION CHECK KIT
K813431 SALICYLATES
Search all 19 clearances from Bio-Analytics Laboratories, Inc. →