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

PRECISE STREP A

K Number: K923673 · Decision Sep 28, 1992
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
104
Applicant Total
10
Review Days
68

Basic Information

Device Name
PRECISE STREP A
K Number
K923673
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BECTON DICKINSON ADVANCED DIAGNOSTICS
Date Received
July 22, 1992
Decision Date
September 28, 1992
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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