DUPEL IONTOPHORESIS SYSTEM— 510(k) K991991

Substantially Equivalent

Empi

FDA 510(k) clearance K991991 for DUPEL IONTOPHORESIS SYSTEM, Substantially Equivalent on 1999-09-10. 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: 1999-06-14
Decision date: 1999-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, 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.