FDA 510(k), K023254, SPEEDICATH
FDA 510(k), K023254, SPEEDICATH
Device Name: SPEEDICATH
Manufacturer:
Device Classification Name: Catheter, Urethral
Regulation Number: 876.5130
Classification Product Code: GBM
Date Received: 09/30/2002
Decision Date: 01/27/2003
Regulation Medical Specialty: Gastroenterology/Urology
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