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

VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 23; VITROS CHEMISTRY PRODUCTS PALB PERFORMANCE VERIFIERS I & II

K Number: K042838 · Decision Dec 9, 2004
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
106
Review Days
56

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Basic Information

Device Name
VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 23; VITROS CHEMISTRY PRODUCTS PALB PERFORMANCE VERIFIERS I & II
K Number
K042838
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho-Clinical Diagnostics, Inc.
Date Received
October 14, 2004
Decision Date
December 9, 2004
Product Code
JIT
Advisory Committee
Clinical Chemistry
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
JIT Calibrator, Secondary

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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. →