FUJIFILM 600 SERIES ENDOSCOPES— 510(k) K132210

Name: FDA 510(k) clearance K132210
Creator: U.S. Food and Drug Administration
Published: 2014-01-10

Substantially Equivalent

Fujifilm Medical Systems U.S.A, Inc.

FDA 510(k) clearance K132210 for FUJIFILM 600 SERIES ENDOSCOPES, Substantially Equivalent on 2014-01-10. Applicant: Fujifilm Medical Systems U.S.A, Inc.. Device class: 2.

Clearance details

Applicant: Fujifilm Medical Systems U.S.A, Inc.
Product code: Code FDF
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2013-07-16
Decision date: 2014-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayne, NJ, 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.