FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

VITROS Immunodiagnostic Products Syphilis Reagent Pack

K Number: K241534 · Decision Aug 28, 2024
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
34
Applicant Total
16
Review Days
90

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Basic Information

Device Name
VITROS Immunodiagnostic Products Syphilis Reagent Pack
K Number
K241534
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho Clinical Diagnostics
Date Received
May 30, 2024
Decision Date
August 28, 2024
Product Code
LIP
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
LIP Enzyme Linked Immunoabsorption Assay, Treponema Pallidum

Similar 510(k) Clearances

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

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Other Clearances by Ortho Clinical Diagnostics

K Number Device Name
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K231525 VITROS Immunodiagnostic Products CA 19-9TM Reagent Pack
K221355 VITROS Immuodiagnostic Products CA 125 II Reagent Pack
K213626 VITROS AFP
K212648 VITROS Immunodiagnostic Products CK-MB Reagent Pack
K201312 VITROS Immunodiagnostic Products NT-proBNP II Reagent Pack
K200236 VITROS BRAHMS PCT Reagent Pack and Calibrators
K163433 VITROS Chemistry Products GLU Slides
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