PROGREAT— 510(k) K033913

Substantially Equivalent

Terumo Medical Corp.

FDA 510(k) clearance K033913 for PROGREAT, Substantially Equivalent on 2004-03-11. Applicant: Terumo Medical Corp..

Clearance details

Applicant: Terumo Medical Corp.
Product code: Code KRA
Advisory panel: Cardiovascular
Date received: 2003-12-17
Decision date: 2004-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elkton, MD, US

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.