FDA 510(k)

SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE

K-Number: K970247 · 1997-03-21

Decision Date1997-03-21

Product CodeEOB

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE 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 1997-03-21 under 510(k) number K970247. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE?

SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1997-03-21. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K970247.

When did SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE receive FDA 510(k) clearance?

SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE received FDA 510(k) clearance on 1997-03-21, under 510(k) number K970247.

Who is the listed applicant for SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE?

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 IMAGES ARTHROSCOPE/ENT ENDOSCOPE?

The FDA product code for SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE is EOB.

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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.