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FDA 510(k)

TURBINATE NASAL SPLINT

K-Number: K921202 · 1992-07-23

ApplicantSmith & Nephew Richards, Inc.
Decision Date1992-07-23
Product CodeLYA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TURBINATE NASAL SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Richards, Inc.. It received FDA 510(k) clearance on 1992-07-23 under 510(k) number K921202. The device is classified under product code LYA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURBINATE NASAL SPLINT?

TURBINATE NASAL SPLINT is a medical device that received FDA 510(k) clearance on 1992-07-23. The listed applicant is Smith & Nephew Richards, Inc.. The 510(k) number is K921202.

When did TURBINATE NASAL SPLINT receive FDA 510(k) clearance?

TURBINATE NASAL SPLINT received FDA 510(k) clearance on 1992-07-23, under 510(k) number K921202.

Who is the listed applicant for TURBINATE NASAL SPLINT?

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

What is the FDA product code for TURBINATE NASAL SPLINT?

The FDA product code for TURBINATE NASAL SPLINT is LYA.

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Other records listing Smith & Nephew Richards, 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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