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FDA 510(k)

ENDOTRACHEAL SUCTIONTUBE

K-Number: K913876 · 1992-03-06

ApplicantWillowtech
Decision Date1992-03-06
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ENDOTRACHEAL SUCTIONTUBE is the device name listed in this FDA 510(k) record. The listed applicant is Willowtech. It received FDA 510(k) clearance on 1992-03-06 under 510(k) number K913876. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOTRACHEAL SUCTIONTUBE?

ENDOTRACHEAL SUCTIONTUBE is a medical device that received FDA 510(k) clearance on 1992-03-06. The listed applicant is Willowtech. The 510(k) number is K913876.

When did ENDOTRACHEAL SUCTIONTUBE receive FDA 510(k) clearance?

ENDOTRACHEAL SUCTIONTUBE received FDA 510(k) clearance on 1992-03-06, under 510(k) number K913876.

Who is the listed applicant for ENDOTRACHEAL SUCTIONTUBE?

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

What is the FDA product code for ENDOTRACHEAL SUCTIONTUBE?

The FDA product code for ENDOTRACHEAL SUCTIONTUBE is JOL.

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Related Devices (Code: JOL)

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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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