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

VIDAS CLOSTRIDIUM DIFFICILE TOXIN A (CDA) ASSAY

K Number: K905211 · Decision Oct 11, 1991
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
41
Applicant Total
39
Review Days
325

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Basic Information

Device Name
VIDAS CLOSTRIDIUM DIFFICILE TOXIN A (CDA) ASSAY
K Number
K905211
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Vitek Systems, Inc.
Date Received
November 20, 1990
Decision Date
October 11, 1991
Product Code
LLH
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
LLH Reagents, Clostridium Difficile Toxin

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Other Clearances by Vitek Systems, Inc.

K Number Device Name
K920661 VIDAS CMV IGG ASSAY
K921302 VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM
K921176 VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM
K920952 VITEK IMMUNODIAG ASSAY SYST(VIDAS) FERRITINE ASSAY
K915884 VIDAS CHLAMYDIA ASSAY, MODIFICATION
K912371 BIOMERIEUX RSV DIRECT IF KIT
K910230 LYME-SPOT IF KIT
K910210 SLIDEX MENINGITE-KIT 5
K910304 RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIA
K911429 VITEK GRAM NEGATIVE IDENTIFICATION CARD, MODIFIED
Search all 39 clearances from Vitek Systems, Inc. →