IONTOPHORESIS DEVICE— 510(k) K903093

Unknown

Empi

FDA 510(k) clearance K903093 for IONTOPHORESIS DEVICE, Unknown on 1990-10-11. 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: 1990-07-13
Decision date: 1990-10-11
Decision: Unknown
Clearance type: Traditional
Location: Arden Hills, 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.