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

ACS FRT4 IMMUNOASSAY

K Number: K961510 · Decision Jun 17, 1996
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
125
Review Days
59

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Basic Information

Device Name
ACS FRT4 IMMUNOASSAY
K Number
K961510
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ciba Corning Diagnostics Corp.
Date Received
April 19, 1996
Decision Date
June 17, 1996
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)

Similar 510(k) Clearances

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K Number Device Name
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K961657 CIBA CORNING 400 SYSTEM
K962021 CIBA CORNING 348 SYSTEM
K962126 ACS CKMB II IMMUNOASSAY
K962041 ACS LH2 IMMUNOASSAY
K960246 LIQUID CARDIAC MARKER 1,2,3 ASSAYED
K955873 ACS PHENYTOIN ASSAY
K954697 CIBA CORNING ACS ESTRADIOL-6 ASSAY
Search all 125 clearances from Ciba Corning Diagnostics Corp. →