MODIFICATION TO THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM— 510(k) K093187

Name: FDA 510(k) clearance K093187
Creator: U.S. Food and Drug Administration
Published: 2009-11-05

Substantially Equivalent

Avantis Medical Systems, Inc.

FDA 510(k) clearance K093187 for MODIFICATION TO THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM, Substantially Equivalent on 2009-11-05. Applicant: Avantis Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Avantis Medical Systems, Inc.
Product code: Code FDF
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2009-10-09
Decision date: 2009-11-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FDF

product code FDF

Death: 8
Injury: 729
Malfunction: 61,773
Total: 62,510

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.