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

AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES

K Number: K932178 · Decision Sep 21, 1993
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
41
Review Days
139

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Basic Information

Device Name
AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES
K Number
K932178
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tosoh Medics, Inc.
Date Received
May 5, 1993
Decision Date
September 21, 1993
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)

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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
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