TBD, EMPI BUFFERED IONTOPHORESIS ELECTRODED MDL. 3— 510(k) K912015

Name: FDA 510(k) clearance K912015
Creator: U.S. Food and Drug Administration
Published: 1991-11-15

Substantially Equivalent

Empi

FDA 510(k) clearance K912015 for TBD, EMPI BUFFERED IONTOPHORESIS ELECTRODED MDL. 3, Substantially Equivalent on 1991-11-15. Applicant: Empi. Device class: 2.

Clearance details

Applicant: Empi
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 1991-05-06
Decision date: 1991-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arden Hills, MN, US

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