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

BACTIGEN GROUP B STREPTOCOCCUS-CS TEST

K Number: K872114 · Decision Aug 27, 1987
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
104
Applicant Total
65
Review Days
87

Basic Information

Device Name
BACTIGEN GROUP B STREPTOCOCCUS-CS TEST
K Number
K872114
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
ARMKEL, LLC.
Date Received
June 1, 1987
Decision Date
August 27, 1987
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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