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FDA 510(k), K871869, MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.
FDA 510(k), K871869, MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.
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510(K) Number: K871869
Device Name: MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.
Manufacturer: COATS, MD
Device Classification Name: Device, Iontophoresis, Other Uses
Regulation Number: EGJ
Classification Product Code: KXA
Date Received: 05/13/1987
Decision Date: 08/11/1987
Decision Date: Substantially Equivalent - With Drug (SESD)
Regulation Medical Specialty: Physical Medicine
Device Name: MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.
Manufacturer: COATS, MD
Device Classification Name: Device, Iontophoresis, Other Uses
Regulation Number: EGJ
Classification Product Code: KXA
Date Received: 05/13/1987
Decision Date: 08/11/1987
Decision Date: Substantially Equivalent - With Drug (SESD)
Regulation Medical Specialty: Physical Medicine
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