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FDA 510(k), K070085, BALANCE REHABILITATION UNIT (BRU)
FDA 510(k), K070085, BALANCE REHABILITATION UNIT (BRU)
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510(K) Number: K070085
Device Name: BALANCE REHABILITATION UNIT (BRU)
Manufacturer: MEDICAA (URUGUAY) S.A.
Device Classification Name: apparatus, vestibular analysis
Regulation Number:
Classification Product Code: LXV
Date Received: 01/09/2007
Decision Date: 02/26/2007
Regulation Medical Specialty:
Device Name: BALANCE REHABILITATION UNIT (BRU)
Manufacturer: MEDICAA (URUGUAY) S.A.
Device Classification Name: apparatus, vestibular analysis
Regulation Number:
Classification Product Code: LXV
Date Received: 01/09/2007
Decision Date: 02/26/2007
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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