ENDO FLIP— 510(k) K102214

Substantially Equivalent

Crospon, Ltd.

FDA 510(k) clearance K102214 for ENDO FLIP, Substantially Equivalent on 2010-12-16. Applicant: Crospon, Ltd..

Clearance details

Applicant: Crospon, Ltd.
Product code: Code FFX
Advisory panel: Gastroenterology, Urology
Date received: 2010-08-06
Decision date: 2010-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bonita Springs, FL, US

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Adverse events under product code FFX

product code FFX

Other: 1
Total: 1

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.