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FDA 510(k)

ANALYZER, CENTRIFUGAL, IL MULTISTAT III

K-Number: K770660 · 1977-06-24

ApplicantInstrumentation Laboratory CO
Decision Date1977-06-24
Product Code
DecisionSubstantially Equivalent

Device Summary

ANALYZER, CENTRIFUGAL, IL MULTISTAT III 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 1977-06-24 under 510(k) number K770660. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYZER, CENTRIFUGAL, IL MULTISTAT III?

ANALYZER, CENTRIFUGAL, IL MULTISTAT III is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K770660.

When did ANALYZER, CENTRIFUGAL, IL MULTISTAT III receive FDA 510(k) clearance?

ANALYZER, CENTRIFUGAL, IL MULTISTAT III received FDA 510(k) clearance on 1977-06-24, under 510(k) number K770660.

Who is the listed applicant for ANALYZER, CENTRIFUGAL, IL MULTISTAT III?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

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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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