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FDA 510(k)

ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY

K-Number: K932988 · 1993-07-26

ApplicantSmith & Nephew Richards, Inc.
Decision Date1993-07-26
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY 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 1993-07-26 under 510(k) number K932988. 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 ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY?

ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY is a medical device that received FDA 510(k) clearance on 1993-07-26. The listed applicant is Smith & Nephew Richards, Inc.. The 510(k) number is K932988.

When did ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY receive FDA 510(k) clearance?

ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY received FDA 510(k) clearance on 1993-07-26, under 510(k) number K932988.

Who is the listed applicant for ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY?

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 ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY?

The FDA product code for ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY is EOB.

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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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