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

LIPOPROTEIN (A) SPQ III ANTIBODY REAGENT SET

K Number: K993669 · Decision Nov 17, 1999
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
42
Applicant Total
71
Review Days
16

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Basic Information

Device Name
LIPOPROTEIN (A) SPQ III ANTIBODY REAGENT SET
K Number
K993669
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
866.5600
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DiaSorin, Inc.
Date Received
November 1, 1999
Decision Date
November 17, 1999
Product Code
DFC
Advisory Committee
Immunology
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
DFC Lipoprotein, Low-Density, Antigen, Antiserum, Control

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K213858 LIAISON Calprotectin, LIAISON Q.S.E.T. Device Plus
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
Search all 71 clearances from DiaSorin, Inc. →