Bendit2.7 Steerable Microcatheter— 510(k) K200582

Substantially Equivalent

Bend IT Technologies, Ltd.

FDA 510(k) clearance K200582 for Bendit2.7 Steerable Microcatheter, Substantially Equivalent on 2020-06-25. Applicant: Bend IT Technologies, Ltd..

Clearance details

Applicant: Bend IT Technologies, Ltd.
Product code: Code KRA
Advisory panel: Cardiovascular
Date received: 2020-03-06
Decision date: 2020-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Petach Tikva, IL

Download summary PDF View on FDA.gov ↗

Adverse events under product code KRA

product code KRA

Death: 234
Injury: 1,029
Malfunction: 3,012
Other: 2
Total: 4,277

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.