FDA 510(k), K040658, BARDEX I.C. LATEX FOLEY CATHETER

FDA 510(k), K040658, BARDEX I.C. LATEX FOLEY CATHETER

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510(K) Number: K040658
Device Name: BARDEX I.C. LATEX FOLEY CATHETER
Manufacturer: C.R. BARD, INC.
Device Classification Name: catheter, urological (antimicrobial) and accessories
Regulation Number: 876.5130
Classification Product Code: MJC
Date Received: 03/12/2004
Decision Date: 09/29/2004
Regulation Medical Specialty: Gastroenterology/Urology

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