FDA 510(k)

VENTILATION TUBES

K-Number: K960477 · 1996-02-26

Decision Date1996-02-26

Product CodeETD

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

VENTILATION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1996-02-26 under 510(k) number K960477. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTILATION TUBES?

VENTILATION TUBES is a medical device that received FDA 510(k) clearance on 1996-02-26. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K960477.

When did VENTILATION TUBES receive FDA 510(k) clearance?

VENTILATION TUBES received FDA 510(k) clearance on 1996-02-26, under 510(k) number K960477.

Who is the listed applicant for VENTILATION TUBES?

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

What is the FDA product code for VENTILATION TUBES?

The FDA product code for VENTILATION TUBES is ETD.

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Related Devices (Code: ETD)

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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.