MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F— 510(k) K050558

Unknown

C.R. Bard, Inc.

FDA 510(k) clearance K050558 for MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F, Unknown on 2005-08-29. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code DTK
Advisory panel: Cardiovascular
Date received: 2005-03-03
Decision date: 2005-08-29
Decision: Unknown
Clearance type: Traditional
Location: Tempe, AZ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DTK

product code DTK

Death: 208
Injury: 11,286
Malfunction: 3,002
Total: 14,496

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.