MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE— 510(k) K060236

Name: FDA 510(k) clearance K060236
Creator: U.S. Food and Drug Administration
Published: 2006-03-31

Substantially Equivalent

Iomed, Inc.

FDA 510(k) clearance K060236 for MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE, Substantially Equivalent on 2006-03-31. Applicant: Iomed, Inc.. Device class: 2.

Clearance details

Applicant: Iomed, Inc.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2006-01-30
Decision date: 2006-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, 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.