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FDA 510(k)

IL MODEL 1301, PH BLOOD GAS SYSTEM

K-Number: K820744 · 1982-04-15

ApplicantInstrumentation Laboratory CO
Decision Date1982-04-15
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IL MODEL 1301, PH BLOOD GAS SYSTEM 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 1982-04-15 under 510(k) number K820744. 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 IL MODEL 1301, PH BLOOD GAS SYSTEM?

IL MODEL 1301, PH BLOOD GAS SYSTEM is a medical device that received FDA 510(k) clearance on 1982-04-15. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K820744.

When did IL MODEL 1301, PH BLOOD GAS SYSTEM receive FDA 510(k) clearance?

IL MODEL 1301, PH BLOOD GAS SYSTEM received FDA 510(k) clearance on 1982-04-15, under 510(k) number K820744.

Who is the listed applicant for IL MODEL 1301, PH BLOOD GAS SYSTEM?

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 IL MODEL 1301, PH BLOOD GAS SYSTEM?

The FDA product code for IL MODEL 1301, PH BLOOD GAS SYSTEM 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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