WiCap— 510(k) K160582

Substantially Equivalent

Athena Gtx

FDA 510(k) clearance K160582 for WiCap, Substantially Equivalent on 2016-09-02. Applicant: Athena Gtx.

Clearance details

Applicant: Athena Gtx
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 2016-03-01
Decision date: 2016-09-02
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Johnson, IA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQA

product code DQA

Death: 66
Malfunction: 2,867
Other: 1
Total: 2,934

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.