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FDA 510(k), K062833, POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM
FDA 510(k), K062833, POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM
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510(K) Number: K062833
Device Name: POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM
Manufacturer: VIDACARE CORPORATION
Device Classification Name: instrument, biopsy, mechanical, gastrointestinal
Regulation Number: 876.1075
Classification Product Code: FCF
Date Received: 09/21/2006
Decision Date: 11/30/2006
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM
Manufacturer: VIDACARE CORPORATION
Device Classification Name: instrument, biopsy, mechanical, gastrointestinal
Regulation Number: 876.1075
Classification Product Code: FCF
Date Received: 09/21/2006
Decision Date: 11/30/2006
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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