EPIX XL TENS UNIT— 510(k) K951903

Substantially Equivalent

Empi

FDA 510(k) clearance K951903 for EPIX XL TENS UNIT, Substantially Equivalent on 1996-03-20. Applicant: Empi. Device class: 2.

Clearance details

Applicant: Empi
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1995-04-24
Decision date: 1996-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arden Hills, 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.