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FDA 510(k)

IL682, CO-OXIMETER

K-Number: K945677 · 1995-10-20

ApplicantInstrumentation Laboratory CO
Decision Date1995-10-20
Product CodeGKR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

IL682, CO-OXIMETER 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 1995-10-20 under 510(k) number K945677. The device is classified under product code GKR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL682, CO-OXIMETER?

IL682, CO-OXIMETER is a medical device that received FDA 510(k) clearance on 1995-10-20. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K945677.

When did IL682, CO-OXIMETER receive FDA 510(k) clearance?

IL682, CO-OXIMETER received FDA 510(k) clearance on 1995-10-20, under 510(k) number K945677.

Who is the listed applicant for IL682, CO-OXIMETER?

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 IL682, CO-OXIMETER?

The FDA product code for IL682, CO-OXIMETER is GKR.

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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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