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FDA 510(k)

MULTISTAT III CREATININE TEST

K-Number: K771443 · 1977-08-22

ApplicantInstrumentation Laboratory CO
Decision Date1977-08-22
Product CodeCGX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTISTAT III CREATININE 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 1977-08-22 under 510(k) number K771443. The device is classified under product code CGX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTISTAT III CREATININE TEST?

MULTISTAT III CREATININE TEST is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K771443.

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

MULTISTAT III CREATININE TEST received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771443.

Who is the listed applicant for MULTISTAT III CREATININE 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 CREATININE TEST?

The FDA product code for MULTISTAT III CREATININE TEST is CGX.

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Related Devices (Code: CGX)

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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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