StimSox(TM) System— 510(k) K151922

Substantially Equivalent

Stimmed, LLC

FDA 510(k) clearance K151922 for StimSox(TM) System, Substantially Equivalent on 2016-04-15. Applicant: Stimmed, LLC. Device class: 2.

Clearance details

Applicant: Stimmed, LLC
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2015-07-13
Decision date: 2016-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Williamsville, NY, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.