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FDA 510(k)

ENDOTRACHEAL TUBE HOLDER

K-Number: K810737 · 1981-04-17

Decision Date1981-04-17
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ENDOTRACHEAL TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Aircare Systems. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K810737. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOTRACHEAL TUBE HOLDER?

ENDOTRACHEAL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Aircare Systems. The 510(k) number is K810737.

When did ENDOTRACHEAL TUBE HOLDER receive FDA 510(k) clearance?

ENDOTRACHEAL TUBE HOLDER received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810737.

Who is the listed applicant for ENDOTRACHEAL TUBE HOLDER?

The FDA 510(k) record lists Aircare Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOTRACHEAL TUBE HOLDER?

The FDA product code for ENDOTRACHEAL TUBE HOLDER is CBH.

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.

Related Devices (Code: CBH)

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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