Peritoneal Dialysis Tubing Kit
The Peritoneal Dialysis Tubing Kit is a convenience kit containing tubing and associated supplies used in peritoneal dialysis procedures for patients with kidney failure. It is classified as FDA Class 2 under 21 CFR 876.5630 in the Gastroenterology and Urology specialty. Per the FDA's 1997 Convenience Kits Interim Regulatory Guidance, this type of kit is under enforcement discretion and does not require a 510(k) premarket notification if it meets all applicable criteria. Product code PPK; not an implant and not life-sustaining.
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Basic Information
- Product Code
- PPK
- Device Class
- FDA class 2
- Regulation Number
- 876.5630
- Medical Specialty
- Gastroenterology, Urology
- Review Panel
- GU
- Submission Type
- 7
Device Characteristics
Definition
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.
FEI Numbers
This FDA classification entry is associated with 7 FEI numbers. Click on an entry to view related FDA registrations.
Registration Numbers
This FDA classification entry is associated with 7 registration numbers. Click on an entry to view related FDA registrations.