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

CAPILLARYS Hb A1c

K Number: K171861 · Decision Feb 7, 2018
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
25
Applicant Total
32
Review Days
230

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Basic Information

Device Name
CAPILLARYS Hb A1c
K Number
K171861
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1373
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sebia
Date Received
June 22, 2017
Decision Date
February 7, 2018
Product Code
PDJ
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
PDJ Hemoglobin A1c Test System

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Other Clearances by Sebia

K Number Device Name
K232027 CAPI 3 NEONAT Hb, CAPILLARYS 3 DBS Instrument
K231601 FLC Kappa, FLC Lambda,FLC Control Level 1, FLC Control Level 2
K210623 FLC Kappa, FLC Lambda, FLC Control Level 1, FLC Control Level 2
K203184 HYDRASHIFT 2/4 isatuximab
K192095 CAPI 3 Immunotyping, Capillarys 3 Tera
K190851 HYDRASHIFT 2/4 daratumumab
K180762 CAPI 3 HEMOGLOBIN(E)
K172195 HYDRASHIFT 2/4 daratumumab, daratumumab Control
K171537 CAPI 3 Hb A1c
K162281 CAPI 3 Hb A1c, MULTI-SYSTEM Hb A1C CAPILLARY CONTROLS (2)
Search all 32 clearances from Sebia →