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

AIA-PACK C-Peptide Control Set

K Number: K143296 · Decision Dec 16, 2014
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
20
Review Days
29

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Basic Information

Device Name
AIA-PACK C-Peptide Control Set
K Number
K143296
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tosoh Bioscience, Inc.
Date Received
November 17, 2014
Decision Date
December 16, 2014
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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Other Clearances by Tosoh Bioscience, Inc.

K Number Device Name
K250073 Tosoh Automated Glycohemoglobin Analyzer HLC-723GR01
K211199 ST AIA-PACK BNP Assay
K200904 Tosoh Automated Glycohemoglobin Analyzer HLC-723G8
K160113 ST AIA-PACK hsE2 Calibrator Set
K153417 ST AIA-PACK PROG III Calibrator Set
K150270 ST AIA-PACK 25-OH Vitamin D, ST AIA-PACK 25-OH Vitamin D Calibrator Set, AIA-PACK 25-OH Vitamin D Control Set, and ST AIA-PACK 25-OH Vitamin D Pretreatment Set
K143075 ST AIA-PACK SHBG, ST AIA-PACK SHBG Calibrator Set
K143144 ST AIA-PACK PROG II Calibrator Set
K140648 ST AIA-PACK C-PEPTIDE II CALIBRATOR SET
K131580 AUTOMATED GYLCOHEMOGLOBIN ANALYZER HLC-723G8
Search all 20 clearances from Tosoh Bioscience, Inc. →