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

CHOLERA SMART(TM)

K Number: K932622 · Decision Jun 27, 1995
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
2
Applicant Total
10
Review Days
756

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Basic Information

Device Name
CHOLERA SMART(TM)
K Number
K932622
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3930
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
New Horizons Diagnostics Co.
Date Received
June 1, 1993
Decision Date
June 27, 1995
Product Code
GSQ
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
GSQ Antiserum, Vibrio Cholerae, All Varieties

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Other Clearances by New Horizons Diagnostics Co.

K Number Device Name
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
K821362 IMPROVED GONO GEN
K820007 NEISSERIA GONORRHOEAE TEST