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FDA 510(k), K022406, EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET
FDA 510(k), K022406, EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET
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510(K) Number: K022406
Device Name: EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET
Manufacturer: ARMAND HAMID
Device Classification Name: Needle, Hypodermic, Single Lumen
Regulation Number: FMI
Classification Product Code: 07/23/2002
Date Received: 09/30/2002
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET
Manufacturer: ARMAND HAMID
Device Classification Name: Needle, Hypodermic, Single Lumen
Regulation Number: FMI
Classification Product Code: 07/23/2002
Date Received: 09/30/2002
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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