PLEURX PERITONEAL CATHETER SYSTEM— 510(k) K113854

Unknown

Care Fusion

FDA 510(k) clearance K113854 for PLEURX PERITONEAL CATHETER SYSTEM, Unknown on 2012-03-19. Applicant: Care Fusion. Device class: 2.

Clearance details

Applicant
Care Fusion
Product code
Code PNG
Device class
Class 2
Regulation
21 CFR 876.5630
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Unknown
Clearance type
Traditional
Location
Waukegan, IL, US
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