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

VIDAS RESPIRATORY SYNCYTIAL VIRUS (RSV) ASSAY

K Number: K896097 · Decision Feb 26, 1990
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
31
Applicant Total
39
Review Days
129

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Basic Information

Device Name
VIDAS RESPIRATORY SYNCYTIAL VIRUS (RSV) ASSAY
K Number
K896097
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3480
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Vitek Systems, Inc.
Date Received
October 20, 1989
Decision Date
February 26, 1990
Product Code
GQG
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
GQG Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus

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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
K905211 VIDAS CLOSTRIDIUM DIFFICILE TOXIN A (CDA) ASSAY
K912371 BIOMERIEUX RSV DIRECT IF KIT
K910230 LYME-SPOT IF KIT
K910210 SLIDEX MENINGITE-KIT 5
K910304 RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIA
Search all 39 clearances from Vitek Systems, Inc. →