FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

ACE CALIBRATOR

K Number: K141728 · Decision Jul 28, 2014
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
12
Review Days
32

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Basic Information

Device Name
ACE CALIBRATOR
K Number
K141728
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SENTINEL CH. SpA
Date Received
June 26, 2014
Decision Date
July 28, 2014
Product Code
JIT
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
JIT Calibrator, Secondary

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Other Clearances by SENTINEL CH. SpA

K Number Device Name
K242585 Cystatin C
K211058 Lp(a) Ultra
K193001 Albumin BCP
K192118 CRP Vario
K173833 CRP Vario
K102706 CKMB UDR ASSAY
K083602 KAPPA LIGHT CHAINS
K083601 LAMBDA LIGHT CHAINS
K081533 SENTINEL PLASMAPROTEINS CAL 3X
K073634 MULTIGENT CREATININE (ENZYMATIC) ASSAY
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