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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device vascular access port kit
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.
Product CodePXK
Regulation Number 880.5965
Device Class 2

MDR Year MDR Reports MDR Events
2018 1 1
2024 1 1

Device Problems MDRs with this Device Problem Events in those MDRs
Mechanical Problem 1 1
Device Dislodged or Dislocated 1 1
Adverse Event Without Identified Device or Use Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Extravasation 1 1
Foreign Body In Patient 1 1
Device Embedded In Tissue or Plaque 1 1

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