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

VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM (VIDAS) TOXO.

K Number: K900818 · Decision Apr 30, 1990
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
39
Review Days
68

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Basic Information

Device Name
VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM (VIDAS) TOXO.
K Number
K900818
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Vitek Systems, Inc.
Date Received
February 21, 1990
Decision Date
April 30, 1990
Product Code
LGD
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
LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LGD), ordered by most recent decision date.

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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. →