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FDA 510(k), K831320, DRIONIC
FDA 510(k), K831320, DRIONIC
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510(K) Number: K831320
Device Name: DRIONIC
Manufacturer: GENERAL MEDICAL CO.
Device Classification Name: device, iontophoresis, other uses
Regulation Number: 890.5525
Classification Product Code: EGJ
Date Received: 04/22/1983
Decision Date: 07/19/1983
Regulation Medical Specialty: Physical Medicine
Device Name: DRIONIC
Manufacturer: GENERAL MEDICAL CO.
Device Classification Name: device, iontophoresis, other uses
Regulation Number: 890.5525
Classification Product Code: EGJ
Date Received: 04/22/1983
Decision Date: 07/19/1983
Regulation Medical Specialty: Physical Medicine
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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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