DUPEL IONTOPHORESIS DEVICE— 510(k) K915444

Substantially Equivalent

Empi

FDA 510(k) clearance K915444 for DUPEL IONTOPHORESIS DEVICE, Substantially Equivalent on 1994-07-15. 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: 1991-12-05
Decision date: 1994-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arden Hills, MN, US

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K061650 — SELECT TENS, MODEL 4600S2007-01-22

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