FDA 510(k), K101567, SHARPS CONTAINER
FDA 510(k), K101567, SHARPS CONTAINER
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510(K) Number: K101567
Device Name: SHARPS CONTAINER
Manufacturer: CIXI LEINUO PLASTIC CO. LTD
Device Classification Name: container, sharps
Regulation Number: 880.5570
Classification Product Code: MMK
Date Received: 06/04/2010
Decision Date: 09/02/2010
Regulation Medical Specialty: General Hospital
Device Name: SHARPS CONTAINER
Manufacturer: CIXI LEINUO PLASTIC CO. LTD
Device Classification Name: container, sharps
Regulation Number: 880.5570
Classification Product Code: MMK
Date Received: 06/04/2010
Decision Date: 09/02/2010
Regulation Medical Specialty: General Hospital
- 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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