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FDA 510(k), K001337, DANIELS SHARPSMART REUSABLE SHARPS CONTAINER
FDA 510(k), K001337, DANIELS SHARPSMART REUSABLE SHARPS CONTAINER
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510(K) Number: K001337
Device Name: DANIELS SHARPSMART REUSABLE SHARPS CONTAINER
Manufacturer: FLOYD G LARSON
Device Classification Name: Container, Sharps
Regulation Number: MMK
Classification Product Code: 04/27/2000
Date Received: 07/05/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: DANIELS SHARPSMART REUSABLE SHARPS CONTAINER
Manufacturer: FLOYD G LARSON
Device Classification Name: Container, Sharps
Regulation Number: MMK
Classification Product Code: 04/27/2000
Date Received: 07/05/2000
Decision Date: Substantially Equivalent (SESE)
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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