FDA 510(k), K152183, EXELINT SecureTouch Safety Hypodermic Needle
FDA 510(k), K152183, EXELINT SecureTouch Safety Hypodermic Needle
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510(K) Number: K152183
Device Name: EXELINT SecureTouch Safety Hypodermic Needle
Manufacturer: Navid Hamid
Device Classification Name: Needle, Hypodermic, Single Lumen
Regulation Number: FMI
Classification Product Code: 08/05/2015
Date Received: 11/02/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: EXELINT SecureTouch Safety Hypodermic Needle
Manufacturer: Navid Hamid
Device Classification Name: Needle, Hypodermic, Single Lumen
Regulation Number: FMI
Classification Product Code: 08/05/2015
Date Received: 11/02/2015
Decision Date: Substantially Equivalent (SESE)
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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