PolyCatch Retrieval Device— 510(k) K142258

Substantially Equivalent

Medi-Globe Corporation

FDA 510(k) clearance K142258 for PolyCatch Retrieval Device, Substantially Equivalent on 2014-09-30. Applicant: Medi-Globe Corporation.

Clearance details

Applicant: Medi-Globe Corporation
Product code: Code FDI
Advisory panel: Gastroenterology, Urology
Date received: 2014-08-14
Decision date: 2014-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tempe, AZ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FDI

product code FDI

Death: 6
Injury: 217
Malfunction: 1,544
Total: 1,767

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.