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FDA 510(k)

SMITH & NEPHEW INSTRUMENT TRAYS

K-Number: K091627 · 2009-07-02

ApplicantSmith & Nephew, Inc.
Decision Date2009-07-02
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW INSTRUMENT TRAYS 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 2009-07-02 under 510(k) number K091627. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW INSTRUMENT TRAYS?

SMITH & NEPHEW INSTRUMENT TRAYS is a medical device that received FDA 510(k) clearance on 2009-07-02. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K091627.

When did SMITH & NEPHEW INSTRUMENT TRAYS receive FDA 510(k) clearance?

SMITH & NEPHEW INSTRUMENT TRAYS received FDA 510(k) clearance on 2009-07-02, under 510(k) number K091627.

Who is the listed applicant for SMITH & NEPHEW INSTRUMENT TRAYS?

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 SMITH & NEPHEW INSTRUMENT TRAYS?

The FDA product code for SMITH & NEPHEW INSTRUMENT TRAYS is KCT.

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Other records listing Smith & Nephew, Inc. as applicant

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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.

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