FDA 510(k), K062792, ERCHONIA IOTO_240

FDA 510(k), K062792, ERCHONIA IOTO_240

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510(K) Number: K062792
Device Name: ERCHONIA IOTO_240
Manufacturer: ERCHONIA MEDICAL, INC.
Device Classification Name: device, iontophoresis, other uses
Regulation Number: 890.5525
Classification Product Code: EGJ
Date Received: 09/18/2006
Decision Date: 03/01/2007
Regulation Medical Specialty: Physical Medicine
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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