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FDA 510(k)

IL TEST PLASMIN INHIBITOR

K-Number: K981696 · 1998-08-27

ApplicantInstrumentation Laboratory CO
Decision Date1998-08-27
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

IL TEST PLASMIN INHIBITOR 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 1998-08-27 under 510(k) number K981696. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL TEST PLASMIN INHIBITOR?

IL TEST PLASMIN INHIBITOR is a medical device that received FDA 510(k) clearance on 1998-08-27. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K981696.

When did IL TEST PLASMIN INHIBITOR receive FDA 510(k) clearance?

IL TEST PLASMIN INHIBITOR received FDA 510(k) clearance on 1998-08-27, under 510(k) number K981696.

Who is the listed applicant for IL TEST PLASMIN INHIBITOR?

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 IL TEST PLASMIN INHIBITOR?

The FDA product code for IL TEST PLASMIN INHIBITOR is GGP.

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Other records listing Instrumentation Laboratory CO as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K221359ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgMK223187HemosIL Liquid Anti-XaK223090GEM Premier ChemSTATK223402HemosIL von Willebrand Factor AntigenK213464HemosIL Liquid Anti-XaK213426HemosIL ReadiPlasTin

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Related Devices (Code: GGP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251440CRYOcheck Chromogenic Factor VIIIPrecision Biologic, Inc.K230852HemosIL Chromogenic Factor IXInstrumentation Laboratory CompanyK220728vWF AgSiemens Healthcare Diagnostics Products GmbHK214002CRYOcheck Chromogenic Factor IXPrecision Biologic, Inc.K223402HemosIL von Willebrand Factor AntigenInstrumentation Laboratory COK200033HemosIL von Willebrand Factor AntigenInstrumentation Laboratory CO

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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