DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE— 510(k) K894549

Unknown

Henley Intl.

FDA 510(k) clearance K894549 for DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE, Unknown on 1990-02-09. Applicant: Henley Intl.. Device class: 2.

Clearance details

Applicant: Henley Intl.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 1989-07-20
Decision date: 1990-02-09
Decision: Unknown
Clearance type: Traditional
Location: Sugar Land, TX, 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.