FLEXIBLE ENDOSCOPE 91-8200(90) AND 91-82100(135)— 510(k) K884631

Name: FDA 510(k) clearance K884631
Creator: U.S. Food and Drug Administration
Published: 1989-03-22

Substantially Equivalent

Xomed, Inc.

FDA 510(k) clearance K884631 for FLEXIBLE ENDOSCOPE 91-8200(90) AND 91-82100(135), Substantially Equivalent on 1989-03-22. Applicant: Xomed, Inc.. Device class: 1.

Clearance details

Applicant: Xomed, Inc.
Product code: Code LRC
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1988-11-07
Decision date: 1989-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LRC

product code LRC

Death: 5
Total: 5

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.