PPLClass II
Single Needle (co-axial Flow) Dialysis Kit
Gastroenterology, Urology · 21 CFR 876.5820
This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
MDR events3All time
Recalls0All time
Registered firms7Currently listed
510(k) clearances0All time
Recent MDR events
3 adverse event reports on file
Event type breakdown
Injury3
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
7 firms currently registered for this product code
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.