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FDA 510(k)

IL 1312, PH BLOOD GAS MANAGER

K-Number: K842042 · 1984-07-11

ApplicantInstrumentation Laboratory CO
Decision Date1984-07-11
Product Code
DecisionSubstantially Equivalent

Device Summary

IL 1312, PH BLOOD GAS MANAGER 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 1984-07-11 under 510(k) number K842042. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL 1312, PH BLOOD GAS MANAGER?

IL 1312, PH BLOOD GAS MANAGER is a medical device that received FDA 510(k) clearance on 1984-07-11. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K842042.

When did IL 1312, PH BLOOD GAS MANAGER receive FDA 510(k) clearance?

IL 1312, PH BLOOD GAS MANAGER received FDA 510(k) clearance on 1984-07-11, under 510(k) number K842042.

Who is the listed applicant for IL 1312, PH BLOOD GAS MANAGER?

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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Other records listing Instrumentation Laboratory CO as applicant

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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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