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FDA 510(k), K943349, MAHURKAR DUAL LUMEN CATHETER
FDA 510(k), K943349, MAHURKAR DUAL LUMEN CATHETER
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510(K) Number: K943349
Device Name: MAHURKAR DUAL LUMEN CATHETER
Manufacturer: JERRY FREUNDLICH
Device Classification Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation Number: FOZ
Classification Product Code: 07/12/1994
Date Received: 03/22/1995
Decision Date: Substantially Equivalent - Kit (SESK)
Regulation Medical Specialty: General Hospital
Device Name: MAHURKAR DUAL LUMEN CATHETER
Manufacturer: JERRY FREUNDLICH
Device Classification Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation Number: FOZ
Classification Product Code: 07/12/1994
Date Received: 03/22/1995
Decision Date: Substantially Equivalent - Kit (SESK)
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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