FDA 510(k), K863166, MODEL 6110 IONTOPHORETIC APPLICATOR

FDA 510(k), K863166, MODEL 6110 IONTOPHORETIC APPLICATOR

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510(K) Number: K863166
Device Name: MODEL 6110 IONTOPHORETIC APPLICATOR
Manufacturer: COATS, MD
Device Classification Name: Device, Iontophoresis, Other Uses
Regulation Number: EGJ
Classification Product Code: KXA
Date Received: 08/18/1986
Decision Date: 03/04/1987
Decision: Substantially Equivalent (SESE)
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. Learn more about Fast-Track Requests here.

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