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

VITROS IMMUNODIAGNOSTIC PRODUCTS PSA CALIBRATORS, VITROS IMMUNODIAGNOSTIC PRODUCTS PSA REAGENT PACK

K Number: K984289 · Decision Mar 12, 1999
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
33
Applicant Total
106
Review Days
101

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Basic Information

Device Name
VITROS IMMUNODIAGNOSTIC PRODUCTS PSA CALIBRATORS, VITROS IMMUNODIAGNOSTIC PRODUCTS PSA REAGENT PACK
K Number
K984289
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.6010
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho-Clinical Diagnostics, Inc.
Date Received
December 1, 1998
Decision Date
March 12, 1999
Product Code
LTJ
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LTJ Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

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K210858 VITROS Chemistry Products PHBR Slides
K191316 VITROS XT Chemistry Products ALB-TP Slides
K190807 VITROS XT Chemistry Products TBIL-ALKP Slides
K190520 VITROS XT Chemistry Products GLU-Ca Slides
K190490 VITROS XT Chemistry Products TRIG-CHOL Slides
K190326 VITROS XT Chemistry Products UREA-CREA Slides
K182063 VITROS Chemistry Products CRBM Slides, VITROS Chemistry Products CREA Slides, VITROS Chemistry Products TBIL Slides, VITROS XT 7600 Integrated System
Search all 106 clearances from Ortho-Clinical Diagnostics, Inc. →