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

REDITEST STREP A TEST KIT

K Number: K903194 · Decision Aug 22, 1990
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
104
Applicant Total
340
Review Days
34

Basic Information

Device Name
REDITEST STREP A TEST KIT
K Number
K903194
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
BOEHRINGER MANNHEIM CORP.
Date Received
July 19, 1990
Decision Date
August 22, 1990
Product Code
GTZ
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
GTZ Antisera, All Groups, Streptococcus Spp.

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