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

AIA-PACK BRCA, ST AIA PACK BRCA

K Number: K010796 · Decision Aug 16, 2001
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
27
Applicant Total
41
Review Days
153

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Basic Information

Device Name
AIA-PACK BRCA, ST AIA PACK BRCA
K Number
K010796
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
March 16, 2001
Decision Date
August 16, 2001
Product Code
MOI
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
MOI System, Test, Immunological, Antigen, Tumor

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Other Clearances by Tosoh Medics, Inc.

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
K992365 AIA-PACK FOLATE ASSAY
K990431 AIA-PACK CA 125
K991252 AIA-PACK FT3 ASSAY
Search all 41 clearances from Tosoh Medics, Inc. →