FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

skyla Hi Hemoglobin A1c System (skyla Hi Analyzer and skyla Hi Hemoglobin A 1 c Reagent Kit)

K Number: K173127 · Decision Sep 25, 2018
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
1
Review Days
361

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Basic Information

Device Name
skyla Hi Hemoglobin A1c System (skyla Hi Analyzer and skyla Hi Hemoglobin A 1 c Reagent Kit)
K Number
K173127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Skyla Corporation H.S.P.B
Date Received
September 29, 2017
Decision Date
September 25, 2018
Product Code
LCP
Advisory Committee
Hematology
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
LCP Assay, Glycosylated Hemoglobin

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