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FDA 510(k), K060814, DYNATRON ION IONTOPHORESIS ELECTRODE
FDA 510(k), K060814, DYNATRON ION IONTOPHORESIS ELECTRODE
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510(K) Number: K060814
Device Name: DYNATRON ION IONTOPHORESIS ELECTRODE
Manufacturer: DYNATRONICS CORP.
Device Classification Name: device, iontophoresis, other uses
Regulation Number: 890.5525
Classification Product Code: EGJ
Date Received: 03/27/2006
Decision Date: 06/14/2006
Regulation Medical Specialty: Physical Medicine
Device Name: DYNATRON ION IONTOPHORESIS ELECTRODE
Manufacturer: DYNATRONICS CORP.
Device Classification Name: device, iontophoresis, other uses
Regulation Number: 890.5525
Classification Product Code: EGJ
Date Received: 03/27/2006
Decision Date: 06/14/2006
Regulation Medical Specialty: Physical Medicine
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- 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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