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FDA 510(k), K043143, SAFEPICO
FDA 510(k), K043143, SAFEPICO
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510(K) Number: K043143
Device Name: SAFEPICO
Manufacturer: RADIOMETER MEDICAL APS
Device Classification Name: Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation Number: 862.1675
Classification Product Code: JKA
Date Received: 11/15/2004
Decision Date: 04/22/2005
Regulation Medical Specialty: Clinical Chemistry
Device Name: SAFEPICO
Manufacturer: RADIOMETER MEDICAL APS
Device Classification Name: Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation Number: 862.1675
Classification Product Code: JKA
Date Received: 11/15/2004
Decision Date: 04/22/2005
Regulation Medical Specialty: Clinical Chemistry
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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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