FREQUENCER— 510(k) K103176

Substantially Equivalent

Dymedso, Inc.

FDA 510(k) clearance K103176 for FREQUENCER, Substantially Equivalent on 2011-01-26. Applicant: Dymedso, Inc..

Clearance details

Applicant: Dymedso, Inc.
Product code: Code BYI
Advisory panel: Anesthesiology
Date received: 2010-10-28
Decision date: 2011-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Springfield, VT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code BYI

product code BYI

Death: 3
Total: 3

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.