FDA 510(k)

TRACHEOSTOMY TUBE AND TUBE CUFF

K-Number: K924660 · 1992-12-11

Decision Date1992-12-11

Product CodeJOH

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

TRACHEOSTOMY TUBE AND TUBE CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources. It received FDA 510(k) clearance on 1992-12-11 under 510(k) number K924660. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACHEOSTOMY TUBE AND TUBE CUFF?

TRACHEOSTOMY TUBE AND TUBE CUFF is a medical device that received FDA 510(k) clearance on 1992-12-11. The listed applicant is Applied Medical Resources. The 510(k) number is K924660.

When did TRACHEOSTOMY TUBE AND TUBE CUFF receive FDA 510(k) clearance?

TRACHEOSTOMY TUBE AND TUBE CUFF received FDA 510(k) clearance on 1992-12-11, under 510(k) number K924660.

Who is the listed applicant for TRACHEOSTOMY TUBE AND TUBE CUFF?

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

What is the FDA product code for TRACHEOSTOMY TUBE AND TUBE CUFF?

The FDA product code for TRACHEOSTOMY TUBE AND TUBE CUFF is JOH.

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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.