RHYTHMIA MAPPING CATHETER— 510(k) K122461

Substantially Equivalent

Rhythmia Medical, Inc.

FDA 510(k) clearance K122461 for RHYTHMIA MAPPING CATHETER, Substantially Equivalent on 2013-04-18. Applicant: Rhythmia Medical, Inc..

Clearance details

Applicant: Rhythmia Medical, Inc.
Product code: Code DRF
Advisory panel: Cardiovascular
Date received: 2012-08-13
Decision date: 2013-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DRF

product code DRF

Death: 127
Injury: 1,676
Malfunction: 2,003
Other: 1
Total: 3,807

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.