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FDA 510(k)

IL TEST(TM) PRO-CHROM

K-Number: K924884 · 1993-01-14

ApplicantInstrumentation Laboratory CO
Decision Date1993-01-14
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

IL TEST(TM) PRO-CHROM 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 1993-01-14 under 510(k) number K924884. 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(TM) PRO-CHROM?

IL TEST(TM) PRO-CHROM is a medical device that received FDA 510(k) clearance on 1993-01-14. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K924884.

When did IL TEST(TM) PRO-CHROM receive FDA 510(k) clearance?

IL TEST(TM) PRO-CHROM received FDA 510(k) clearance on 1993-01-14, under 510(k) number K924884.

Who is the listed applicant for IL TEST(TM) PRO-CHROM?

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(TM) PRO-CHROM?

The FDA product code for IL TEST(TM) PRO-CHROM 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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