FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

QUANTASE TOTAL GALACTOSE SCREENING ASSAY

K Number: K990644 · Decision Jun 21, 1999
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
8
Applicant Total
4
Review Days
115

Basic Information

Device Name
QUANTASE TOTAL GALACTOSE SCREENING ASSAY
K Number
K990644
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1310
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
QUANTASE LTD.
Date Received
February 26, 1999
Decision Date
June 21, 1999
Product Code
JIA
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
JIA Enzymatic Methods, Galactose

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K Number Device Name
K000754 QUANTASE PHENYLALANINE SCREENING ASSAY 500 TEST KIT
K990654 QUANTASE TOTAL GALACTOSE SCREENING ASSAY 500 TEST KIT
K984463 QUANTASE PHE/GAL SCREENING ASSAY