POLYGRAM NET BIOFEEDBACK APPLICATION— 510(k) K041244

Name: FDA 510(k) clearance K041244
Creator: U.S. Food and Drug Administration
Published: 2004-08-12

Substantially Equivalent

Medtronic Vascular

FDA 510(k) clearance K041244 for POLYGRAM NET BIOFEEDBACK APPLICATION, Substantially Equivalent on 2004-08-12. Applicant: Medtronic Vascular. Device class: 2.

Clearance details

Applicant: Medtronic Vascular
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 2004-05-11
Decision date: 2004-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shoreview, MN, 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.