P-POD— 510(k) K133397

Substantially Equivalent

P-Pod

FDA 510(k) clearance K133397 for P-POD, Substantially Equivalent on 2014-04-18. Applicant: P-Pod. Device class: 2.

Clearance details

Applicant: P-Pod
Product code: Code MVA
Device class: Class 2
Regulation: 21 CFR 882.5970
Advisory panel: Neurology
Date received: 2013-11-06
Decision date: 2014-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodstock, GA, 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.