DeviceClearance

DERMATRON IONTOPHORESIS DEVICE— 510(k) K780310

Substantially Equivalent

Motion Control, Inc.

FDA 510(k) clearance K780310 for DERMATRON IONTOPHORESIS DEVICE, Substantially Equivalent on 1978-07-31. Applicant: Motion Control, Inc..

Clearance details

Applicant
Motion Control, Inc.
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Walker, MI, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.