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

ELIA SYMPHONY IMMUNOASSAY, ANA CONTROL, MODEL 14-55508-01,83-1004-01

K Number: K072149 · Decision Jan 15, 2008
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
179
Applicant Total
22
Review Days
165

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Basic Information

Device Name
ELIA SYMPHONY IMMUNOASSAY, ANA CONTROL, MODEL 14-55508-01,83-1004-01
K Number
K072149
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Phadia US, Inc.
Date Received
August 3, 2007
Decision Date
January 15, 2008
Product Code
LLL
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
LLL Extractable Antinuclear Antibody, Antigen And Control

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Other Clearances by Phadia US, Inc.

K Number Device Name
K141375 ELIA M2; IMMUNOASSAY, POSITIVE CONTROL 100, POSITIVE CONTROL 250
K140225 ELIA PR3S IMMUNOASSAY, ELIA MPOS IMMUNOASSAY, ELIA GBM IMMUNOASSAY, ELIA ANCA/GBM POSITIVE CONTROL 100, ELIA ANCA/GBM PO
K132631 EIA SMDP IMMUNOASSAY
K131821 ELIA(TM) CARDIOLIPIN IGA IMMUNOASSAY
K122197 AUTOMATED IN VITRO QUANTITATIVE ASSAY FOR THE MEASUREMENT OF ALLERGEN SPECIFIC IGE ANTIBODIES
K113841 IMMUNOCAP ALLERGEN COMPONENTS BUNDLE
K112414 ELIA B2-GLYCOPROTEIN I IGA IMMUNOASSAY
DEN120001 IMMUNOCAP TRYPTASE, CALIBRATORS, CURVE CONTROL, CONJUGATE 50, CALIBRATOR STRIP, CURVE CONTROL STRIP, ANTI-TRYPTASE
K111919 IMMUNOCAP SPECIFIC IGE ALLERGEN BUNDLE, 12 ALLERGEN COMPONENTS
K102673 RHEUMATOID FACTOR IMMUNOLOGICAL TEST SYSTEM
Search all 22 clearances from Phadia US, Inc. →