FDA 510(k), K895768, EXEL SAFELET CATHETER
FDA 510(k), K895768, EXEL SAFELET CATHETER
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510(K) Number: K895768
Device Name: EXEL SAFELET CATHETER
Manufacturer: ESHAGH HAMID
Device Classification Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation Number: FOZ
Classification Product Code: 09/26/1989
Date Received: 02/16/1990
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: EXEL SAFELET CATHETER
Manufacturer: ESHAGH HAMID
Device Classification Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation Number: FOZ
Classification Product Code: 09/26/1989
Date Received: 02/16/1990
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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