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FDA 510(k), K052195, EZ-MIO MANUAL DRIVER
FDA 510(k), K052195, EZ-MIO MANUAL DRIVER
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$149.00 USD
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510(K) Number: K052195
Device Name: EZ-MIO MANUAL DRIVER
Manufacturer: VIDACARE CORPORATION
Device Classification Name: needle, hypodermic, single lumen
Regulation Number: 880.5570
Classification Product Code: FMI
Date Received: 08/11/2005
Decision Date: 11/02/2005
Regulation Medical Specialty: General Hospital
Device Name: EZ-MIO MANUAL DRIVER
Manufacturer: VIDACARE CORPORATION
Device Classification Name: needle, hypodermic, single lumen
Regulation Number: 880.5570
Classification Product Code: FMI
Date Received: 08/11/2005
Decision Date: 11/02/2005
Regulation Medical Specialty: General Hospital
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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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