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FDA 510(k)

MODIFICATION OF ACL ADVANCE

K-Number: K002400 · 2000-08-30

ApplicantInstrumentation Laboratory CO
Decision Date2000-08-30
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF ACL ADVANCE is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 2000-08-30 under 510(k) number K002400. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION OF ACL ADVANCE?

MODIFICATION OF ACL ADVANCE is a medical device that received FDA 510(k) clearance on 2000-08-30. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K002400.

When did MODIFICATION OF ACL ADVANCE receive FDA 510(k) clearance?

MODIFICATION OF ACL ADVANCE received FDA 510(k) clearance on 2000-08-30, under 510(k) number K002400.

Who is the listed applicant for MODIFICATION OF ACL ADVANCE?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION OF ACL ADVANCE?

The FDA product code for MODIFICATION OF ACL ADVANCE is JPA.

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Related Devices (Code: JPA)

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K253658STA Satellite Max®Diagnostica Stago, Inc.K250965Automated Blood Coagulation Analyzer CN-Series (CN-6000)Sysmex America, Inc.K251024TEG 6s Hemostasis System Citrated: K, KH, RT, FF Assay CartridgeHaemoneticsK243858TEG 6s Hemostasis System Citrated: K, KH, RT, FF Assay CartridgeHaemonetics CorporationK232018Citrated: K, KH, RTH, FFHHaemonetics CorporationK233790ACL TOP 970 CLInstrumentation Laboratory

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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