FDA 510(k)

SMITH & NEPHEW DAYLIGHTER(TM)

K-Number: K873786 · 1987-10-23

Decision Date1987-10-23

Product CodeFSY

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW DAYLIGHTER(TM) 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 1987-10-23 under 510(k) number K873786. The device is classified under product code FSY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW DAYLIGHTER(TM)?

SMITH & NEPHEW DAYLIGHTER(TM) is a medical device that received FDA 510(k) clearance on 1987-10-23. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K873786.

When did SMITH & NEPHEW DAYLIGHTER(TM) receive FDA 510(k) clearance?

SMITH & NEPHEW DAYLIGHTER(TM) received FDA 510(k) clearance on 1987-10-23, under 510(k) number K873786.

Who is the listed applicant for SMITH & NEPHEW DAYLIGHTER(TM)?

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 DAYLIGHTER(TM)?

The FDA product code for SMITH & NEPHEW DAYLIGHTER(TM) is FSY.

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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.