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

TOXOSTAT M TEST KIT

K Number: K875113 · Decision Apr 12, 1988
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
30
Review Days
119

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Basic Information

Device Name
TOXOSTAT M TEST KIT
K Number
K875113
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Whittaker Bioproducts, Inc.
Date Received
December 15, 1987
Decision Date
April 12, 1988
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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K Number Device Name
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K904652 LYME STAT M TEST KIT
K904893 FIAX LYME M TEST KIT
K911473 EBNA STAT TEST KIT
K905468 PYLORI-G FIAX TEST KIT
K904738 PYLORI STAT TEST KIT
K901493 FITC MURINE MONOCLONAL ANTI-INFLUENZA TYPE B
K893579 FITC MURINE MONOCLONAL ANTI-INFLUENZA TYPE A
K894932 FIAX EB VCA-M TEST KIT
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