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FDA 510(k), K123300, BD PEN NEEDLE
FDA 510(k), K123300, BD PEN NEEDLE
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$149.00 USD
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510(K) Number: K123300
Device Name: BD PEN NEEDLE
Manufacturer: BECTON DICKINSON & CO.
Device Classification Name: needle, hypodermic, single lumen
Regulation Number: 880.5570
Classification Product Code: FMI
Date Received: 10/23/2012
Decision Date: 01/18/2013
Regulation Medical Specialty: General Hospital
Device Name: BD PEN NEEDLE
Manufacturer: BECTON DICKINSON & CO.
Device Classification Name: needle, hypodermic, single lumen
Regulation Number: 880.5570
Classification Product Code: FMI
Date Received: 10/23/2012
Decision Date: 01/18/2013
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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