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FDA 510(k)

IL 301 TRANSCUTANEOUS OXYGEN MONITOR

K-Number: K822328 · 1982-09-07

Decision Date1982-09-07
Product CodeKLK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IL 301 TRANSCUTANEOUS OXYGEN MONITOR 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 1982-09-07 under 510(k) number K822328. The device is classified under product code KLK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL 301 TRANSCUTANEOUS OXYGEN MONITOR?

IL 301 TRANSCUTANEOUS OXYGEN MONITOR is a medical device that received FDA 510(k) clearance on 1982-09-07. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K822328.

When did IL 301 TRANSCUTANEOUS OXYGEN MONITOR receive FDA 510(k) clearance?

IL 301 TRANSCUTANEOUS OXYGEN MONITOR received FDA 510(k) clearance on 1982-09-07, under 510(k) number K822328.

Who is the listed applicant for IL 301 TRANSCUTANEOUS OXYGEN MONITOR?

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 301 TRANSCUTANEOUS OXYGEN MONITOR?

The FDA product code for IL 301 TRANSCUTANEOUS OXYGEN MONITOR is KLK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Instrumentation Laboratory CO as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: KLK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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