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FDA 510(k), K831000, MEDION MI-200 IONTOPHORETIC MEDICATOR
FDA 510(k), K831000, MEDION MI-200 IONTOPHORETIC MEDICATOR
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510(K) Number: K831000
Device Name: MEDION MI-200 IONTOPHORETIC MEDICATOR
Manufacturer: ETHERINGTON INDUSTRIES
Device Classification Name:
Regulation Number:
Classification Product Code:
Date Received: 03/29/1983
Decision Date: 08/08/1983
Regulation Medical Specialty:
Device Name: MEDION MI-200 IONTOPHORETIC MEDICATOR
Manufacturer: ETHERINGTON INDUSTRIES
Device Classification Name:
Regulation Number:
Classification Product Code:
Date Received: 03/29/1983
Decision Date: 08/08/1983
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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