DYNATRON IBOX IONTOPHORESIS DEVICE— 510(k) K043047

Unknown

Dynatronics Corp.

FDA 510(k) clearance K043047 for DYNATRON IBOX IONTOPHORESIS DEVICE, Unknown on 2005-01-07. Applicant: Dynatronics Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Corp.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2004-11-04
Decision date: 2005-01-07
Decision: Unknown
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.