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FDA 510(k)

ALLEVYN TRACHEOSTOMY DRESSING

K-Number: K890748 · 1989-03-08

Decision Date1989-03-08
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

ALLEVYN TRACHEOSTOMY DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew United, Inc.. It received FDA 510(k) clearance on 1989-03-08 under 510(k) number K890748. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ALLEVYN TRACHEOSTOMY DRESSING?

ALLEVYN TRACHEOSTOMY DRESSING is a medical device that received FDA 510(k) clearance on 1989-03-08. The listed applicant is Smith & Nephew United, Inc.. The 510(k) number is K890748.

When did ALLEVYN TRACHEOSTOMY DRESSING receive FDA 510(k) clearance?

ALLEVYN TRACHEOSTOMY DRESSING received FDA 510(k) clearance on 1989-03-08, under 510(k) number K890748.

Who is the listed applicant for ALLEVYN TRACHEOSTOMY DRESSING?

The FDA 510(k) record lists Smith & Nephew United, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALLEVYN TRACHEOSTOMY DRESSING?

The FDA product code for ALLEVYN TRACHEOSTOMY DRESSING is NAD.

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 Smith & Nephew United, Inc. 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.

View all 34 devices →

Related Devices (Code: NAD)

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

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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