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FDA 510(k)

IL1430 BGELECTROLYTE ANALYZER

K-Number: K935069 · 1994-03-28

ApplicantInstrumentation Laboratory CO
Decision Date1994-03-28
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IL1430 BGELECTROLYTE ANALYZER 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 1994-03-28 under 510(k) number K935069. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL1430 BGELECTROLYTE ANALYZER?

IL1430 BGELECTROLYTE ANALYZER is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K935069.

When did IL1430 BGELECTROLYTE ANALYZER receive FDA 510(k) clearance?

IL1430 BGELECTROLYTE ANALYZER received FDA 510(k) clearance on 1994-03-28, under 510(k) number K935069.

Who is the listed applicant for IL1430 BGELECTROLYTE ANALYZER?

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 IL1430 BGELECTROLYTE ANALYZER?

The FDA product code for IL1430 BGELECTROLYTE ANALYZER is CHL.

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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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