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FDA 510(k), K882980, REBUILDER BUCKET SYSTEM
FDA 510(k), K882980, REBUILDER BUCKET SYSTEM
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510(K) Number: K882980
Device Name: REBUILDER BUCKET SYSTEM
Manufacturer: MICROMED, INC.
Device Classification Name: Stimulator, Nerve, Transcutaneous, For Pain Relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 07/15/1988
Decision Date: 04/24/1989
Regulation Medical Specialty: Neurology
Device Name: REBUILDER BUCKET SYSTEM
Manufacturer: MICROMED, INC.
Device Classification Name: Stimulator, Nerve, Transcutaneous, For Pain Relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 07/15/1988
Decision Date: 04/24/1989
Regulation Medical Specialty: Neurology
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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