Ezee Retrieval— 510(k) K180579
Substantially EquivalentGenicon, Inc.
FDA 510(k) clearance K180579 for Ezee Retrieval, Substantially Equivalent on 2018-03-19. Applicant: Genicon, Inc.. Device class: 2.
Clearance details
- Applicant
- Genicon, Inc.
- Product code
- Product code GCJ
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Winter Park, FL, US
Recent devices under product code GCJ
view allMore clearances from Genicon, Inc.
view allAdverse events under product code GCJ
product code GCJ- Death
- 39
- Injury
- 1,638
- Malfunction
- 28,216
- Other
- 11
- Total
- 29,904
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K180579
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K180579.
Data sourced from openFDA. This site is unofficial and independent of the FDA.