FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

IMPROVED GONO GEN

K Number: K821362 · Decision Aug 4, 1982
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
8
Applicant Total
10
Review Days
89

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Basic Information

Device Name
IMPROVED GONO GEN
K Number
K821362
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3390
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
New Horizons Diagnostics Co.
Date Received
May 7, 1982
Decision Date
August 4, 1982
Product Code
LIC
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
LIC Antiserum, Coagglutination (Direct) Neisseria Gonorrhoeae

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Other Clearances by New Horizons Diagnostics Co.

K Number Device Name
K932622 CHOLERA SMART(TM)
K925190 PYLORISCREEN
K922432 CHOLERASCREEN
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)
K851132 LATEX AGGLUTINATION TEST
K820007 NEISSERIA GONORRHOEAE TEST