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

LATEX AGGLUTINATION TEST

K Number: K851132 · Decision Jul 5, 1985
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
104
Applicant Total
10
Review Days
106

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Basic Information

Device Name
LATEX AGGLUTINATION TEST
K Number
K851132
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
New Horizons Diagnostics Co.
Date Received
March 21, 1985
Decision Date
July 5, 1985
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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K874761 RAPID COLORIMETRIC DIRECT STREP A TEST
K871226 SYPHILIS SEROLOGICAL REAGENTS
K871105 THE GONOGEN II TEST KIT FOR NEISSERIA GONORRHOEAE
K862195 RAPID BACTERIURIA SCREEN (RBS)
K821362 IMPROVED GONO GEN
K820007 NEISSERIA GONORRHOEAE TEST