RSI FEMORAL GUIDING CATHETER— 510(k) K902943

Substantially Equivalent

Retroperfusion Systems, Inc.

FDA 510(k) clearance K902943 for RSI FEMORAL GUIDING CATHETER, Substantially Equivalent on 1990-10-03. Applicant: Retroperfusion Systems, Inc..

Clearance details

Applicant: Retroperfusion Systems, Inc.
Product code: Code DQO
Advisory panel: Cardiovascular
Date received: 1990-07-05
Decision date: 1990-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Costa Mesa, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQO

product code DQO

Death: 35
Injury: 993
Malfunction: 1,772
Other: 5
Total: 2,805

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.