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

THE VITROS 5,1 FS CHEMISTRY SYSTEM

K Number: K041764 · Decision Sep 9, 2004
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
248
Applicant Total
22
Review Days
71

Basic Information

Device Name
THE VITROS 5,1 FS CHEMISTRY SYSTEM
K Number
K041764
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ORTHO-CLINICAL DIAGNOSTICS
Date Received
June 30, 2004
Decision Date
September 9, 2004
Product Code
LCP
Advisory Committee
Hematology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
LCP Assay, Glycosylated Hemoglobin

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K Number Device Name
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K083173 VITROS IMMUNODIAGNOSTIC PRODUCTS TSH REAGENT PACK AND CALIBRATORS, VITROS 3600 IMMUNODIAGNOSTIC SYSTEM
K063720 VITROS IMMUNODIAGNOSTIC PRODUCTS TOTAL B-HCG II REAGENT PACK, CALIBRATORS, RANGE VERIFIERS
K062165 VITROS CHEMISTRY PRODUCTS BARB REAGENT; CALIBRATOR KIT 26; FS CALIBRATOR 1; DAT PERFORMANCE VERIFIERS
K062838 VITROS TROPONIN I ES ASSAY, INCLUDING REAGENT PACK, CALIBRATORS AND RANGE VERIFIERS, MODELS 680 2301, 2302 AND 2303
K060480 VITROS IMMUNODIAGNOSTIC PRODUCTS CORTISOL REAGENT PACK AND CALIBRATORS AND METABOLISM CONTROLS
K052645 VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 28, REF 680 2323; VITROS CHEMISTRY PRODUCTS FS CALIBRATOR 1, REF 6801873;
K042494 VITROS CHEMISTRY PRODUCTS C3 AND CR REAGENT, CALIBRATOR KIT 20, PROTEIN PERFORMANCE VERIFIERS I, II, AND III
K042303 VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS
K033127 VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC CONTROLS
Search all 22 clearances from ORTHO-CLINICAL DIAGNOSTICS →