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FDA 510(k)

MULTISTAT III TOTAL PROTEIN TEST

K-Number: K771476 · 1977-09-12

ApplicantInstrumentation Laboratory CO
Decision Date1977-09-12
Product CodeCEK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTISTAT III TOTAL PROTEIN TEST 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 1977-09-12 under 510(k) number K771476. The device is classified under product code CEK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTISTAT III TOTAL PROTEIN TEST?

MULTISTAT III TOTAL PROTEIN TEST is a medical device that received FDA 510(k) clearance on 1977-09-12. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K771476.

When did MULTISTAT III TOTAL PROTEIN TEST receive FDA 510(k) clearance?

MULTISTAT III TOTAL PROTEIN TEST received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771476.

Who is the listed applicant for MULTISTAT III TOTAL PROTEIN TEST?

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 MULTISTAT III TOTAL PROTEIN TEST?

The FDA product code for MULTISTAT III TOTAL PROTEIN TEST is CEK.

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Related Devices (Code: CEK)

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.

K992846HICHEM TOTAL PROTEIN REAGENTElan Holdings, Inc.K973108TOTAL PROTEIN (MICRO) ASSAY, CATALOGUE NUMBER 450-50Diagnostic Chemicals , Ltd.K980042CARESIDE TOTAL PROTEINExigent Diagnostics, Inc.K971524TOTAL PROTEIN OR TPCarolina Liquid Chemistries Corp.K961864CSF/URINE TOTAL PROTEINTeco DiagnosticsK955905STC DIAGNOSTICS AUTO-LYTE URINARY PROTEIN ASSAYSolarcare Technologies Corp,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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