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..

Clearance details

Applicant: Henley Intl.
Product code: Code EGJ
Advisory panel: Physical Medicine
Date received: 1989-07-20
Decision date: 1990-02-09
Decision: Unknown
Clearance type: Traditional
Location: Sugar Land, TX, US

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