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

ACL TOP FAMILY 50 SERIES: ACL TOP 350 CTS; ACL TOP 550 CTS; ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS

K Number: K150877 · Decision Dec 13, 2015
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
48
Applicant Total
20
Review Days
256

Basic Information

Device Name
ACL TOP FAMILY 50 SERIES: ACL TOP 350 CTS; ACL TOP 550 CTS; ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS
K Number
K150877
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5400
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instrumentation Laboratory Co.
Date Received
April 1, 2015
Decision Date
December 13, 2015
Product Code
GKP
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GKP Instrument, Coagulation, Automated

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