FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LIAISON 25 OH VITAMIN D TOTAL CALIBRATION VERIFIERS, MODEL: 310603

K Number: K090104 · Decision Sep 9, 2009
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
71
Review Days
237

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Basic Information

Device Name
LIAISON 25 OH VITAMIN D TOTAL CALIBRATION VERIFIERS, MODEL: 310603
K Number
K090104
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DiaSorin, Inc.
Date Received
January 15, 2009
Decision Date
September 9, 2009
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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K213936 LIAISON MeMed BV, LIAISON MeMed BV Control Set
K193650 LIAISON Ferritin
K202573 LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus
K202574 LIAISON Lyme IgG, LIAISON Lyme IgG Control Set, LIAISON Lyme Total Antibody Plus
K210272 LIAISON Anti-HAV
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