PIN
- Product code
- PIN
- Device name
- Kidney Perfusion Kit
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.5880
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- Enforcement Discretion
FDA classification 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/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080216.htm. This kit, as described in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market.
Official FDA classification page: PIN
Classification and pathway per current FDA publications. Data from openFDA (CC0).