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FDA 510(k)

IL MODEL 773 FLUORESCENCE LIGHT SCATTER

K-Number: K801026 · 1980-05-28

ApplicantInstrumentation Laboratory CO
Decision Date1980-05-28
Product CodeJJG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IL MODEL 773 FLUORESCENCE LIGHT SCATTER 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 1980-05-28 under 510(k) number K801026. The device is classified under product code JJG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL MODEL 773 FLUORESCENCE LIGHT SCATTER?

IL MODEL 773 FLUORESCENCE LIGHT SCATTER is a medical device that received FDA 510(k) clearance on 1980-05-28. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K801026.

When did IL MODEL 773 FLUORESCENCE LIGHT SCATTER receive FDA 510(k) clearance?

IL MODEL 773 FLUORESCENCE LIGHT SCATTER received FDA 510(k) clearance on 1980-05-28, under 510(k) number K801026.

Who is the listed applicant for IL MODEL 773 FLUORESCENCE LIGHT SCATTER?

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 MODEL 773 FLUORESCENCE LIGHT SCATTER?

The FDA product code for IL MODEL 773 FLUORESCENCE LIGHT SCATTER is JJG.

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Related Devices (Code: JJG)

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.

K972409AG CHEMISTRY ANALYZER SYSTEMLandmark Scientific, Inc.K942782PICCOLO(TM)Abaxis, Inc.K934592EPOC 2000 POINT-OF-CARE ANALYZER AND EPOC 5-CHEMISTRY REAGENT ROTORAbaxis, Inc.K920942OLYMPUS AU800 CLINICAL CHEMISTRY ANALYZEROlympus Corp.K910222COBAS ALPHARoche Diagnostic Systems, Inc.K903626BIOMEK AUTOMATED LABORATORY WORKSTATION W/GENELISABeckman Instruments, Inc.

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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