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

AIA-PACK CA 125

K Number: K990431 · Decision Jun 3, 1999
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
25
Applicant Total
41
Review Days
112

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Basic Information

Device Name
AIA-PACK CA 125
K Number
K990431
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.6010
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tosoh Medics, Inc.
Date Received
February 11, 1999
Decision Date
June 3, 1999
Product Code
LTK
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
LTK Test, Epithelial Ovarian Tumor-Associated Antigen (Ca125)

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K Number Device Name
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K023091 ST AIA-PACK TESTOSTERONE ASSAY
K023891 ST AIA-PACK CA 125 ENZYME IMMUNOASSAY
K020489 G7 AUTOMATED HPLC ANALYZER, BETA-THALASSEMIA MODE
K012820 AIA-PACK CTNI 2ND-GEN ASSAY
K011434 G7 AUTOMATED HPLC ANALYZER
K010796 AIA-PACK BRCA, ST AIA PACK BRCA
K992365 AIA-PACK FOLATE ASSAY
K991252 AIA-PACK FT3 ASSAY
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