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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
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
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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