IONTOPHORESIS DEVICE, MODIFICATION— 510(k) K914621

Unknown

Iomed, Inc.

FDA 510(k) clearance K914621 for IONTOPHORESIS DEVICE, MODIFICATION, Unknown on 1991-12-20. 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: 1991-09-11
Decision date: 1991-12-20
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.