510(k) K113854
K113854 is an FDA 510(k) premarket notification submitted by Care Fusion for the device "PLEURX PERITONEAL CATHETER SYSTEM". The FDA issued a decision of Substantially Equivalent (kit) on March 19, 2012. The device falls under product code PNG (Peritoneal, Drainage Catheter For Refractory Ascites, Long-Term Indwelling), a Class II device regulated under 21 CFR 876.5630. Care Fusion has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESK (Substantially Equivalent (kit))
- Decision Date
- March 19, 2012
- Date Received
- December 29, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Peritoneal, Drainage Catheter For Refractory Ascites, Long-Term Indwelling
- Device Class
- Class II
- Regulation Number
- 876.5630
- Review Panel
- GU
- Submission Type
For drainage of refractory ascites with long-term occurrence from the peritoneal cavity.