TRANSDERM IONTO SYSTEM, MK 2— 510(k) K042590

Name: FDA 510(k) clearance K042590
Creator: U.S. Food and Drug Administration
Published: 2004-10-14

Substantially Equivalent

Mattioli Engineering Corp.

FDA 510(k) clearance K042590 for TRANSDERM IONTO SYSTEM, MK 2, Substantially Equivalent on 2004-10-14. Applicant: Mattioli Engineering Corp.. Device class: 2.

Clearance details

Applicant: Mattioli Engineering Corp.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2004-09-23
Decision date: 2004-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beltsville, MD, US

Download summary PDF View on FDA.gov ↗

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