510(k) K231031

Device
ACL TOP Family 70 Series
Applicant
Instrumentation Laboratory Company
510(k) number
K231031
Product code
GKP
Decision
Substantially Equivalent (SESE)
Decision date
2023-06-21
Date received
2023-04-11
Regulation
864.5400
Classification name
Instrument, Coagulation, Automated
Medical specialty
Hematology
Review panel
Hematology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Carol Marble
Address
180 Hartwell Rd. Bedford MA US 01730 01730

FDA Registration Numbers

Source Documents

510(k) summary PDF

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510(k)DeviceApplicantDecision date
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K160276ACL TOP (ACL TOP 700, ACL TOP 700 CTS, ACL TOP 700 LAS, ACL TOP 500 CTS, ACL TOP 300 CTS)Instrumentation Laboratory CO2016-03-03
K150877ACL TOP FAMILY 50 SERIES: ACL TOP 350 CTS; ACL TOP 550 CTS; ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LASInstrumentation Laboratory CO2015-12-13
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K073377ACL TOP (WITH SYSTEM SOFTWARE V3.0.0)Instrumentation Laboratory CO2008-05-04
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K020979SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL #CA-7000Dade Behring, Inc.2002-06-27
K001645SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-1500Dade Behring, Inc.2000-08-04
K001891MICROSAMPLE COAGULATION ANALYZER, MODEL MCA 310-CBio/Data Corp.2000-07-12
K001145SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-6000Dade Behring, Inc.2000-05-11
K993299SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-1500Dade Behring, Inc.1999-12-07
K993174SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-6000Dade Behring, Inc.1999-11-09