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

VIDAS TOXO IG6 ASSAY (TX6)

K Number: K922737 · Decision May 11, 1993
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
49
Review Days
337

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Basic Information

Device Name
VIDAS TOXO IG6 ASSAY (TX6)
K Number
K922737
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomerieux Vitek, Inc.
Date Received
June 8, 1992
Decision Date
May 11, 1993
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

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Other Clearances by Biomerieux Vitek, Inc.

K Number Device Name
K973819 VIDAS D-DIMER (DD) ASSAY
K972895 VIDAS ROTAVIRUS (RTV) ASSAY
K965092 VIDAS ROTAVIRUS ASSAY
K964887 VIDAS C. DIFFICILE TOXIN A II ASSAY
K955627 VIDAS CHLAMYDIA BLOCKING ASSAY
K962549 VIDAS CREATINE KINASE MB ASSAY 30-421
K962609 GRAM NEGATIVE IDENTIFICATION PLUS CARD
K952095 VITEK GRAM POSITIVE IDENTIFICATION CARD (GPI)
K955647 VIDAS ESTRADIOL II (E2II) ASSAY
K943812 VIDAS LYME SCREEN II
Search all 49 clearances from Biomerieux Vitek, Inc. →