T3 Platform software— 510(k) K202306

Substantially Equivalent

Etiometry, Inc.

FDA 510(k) clearance K202306 for T3 Platform software, Substantially Equivalent on 2020-11-25. Applicant: Etiometry, Inc..

Clearance details

Applicant: Etiometry, Inc.
Product code: Code MWI
Advisory panel: Cardiovascular
Date received: 2020-08-14
Decision date: 2020-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MWI

product code MWI

Death: 16
Malfunction: 963
Total: 979

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.