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

TESTPACK PLUS STREP A

K Number: K922345 · Decision Jul 16, 1992
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
104
Applicant Total
883
Review Days
58

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Basic Information

Device Name
TESTPACK PLUS STREP A
K Number
K922345
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Laboratories
Date Received
May 19, 1992
Decision Date
July 16, 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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