Catheter Repair Kit

Device Code: 2767

Product Code(s): PWR

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.

Device Classification Information

Device Type ID2767
Device NameCatheter Repair Kit
Physical StateThis 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.
Technical MethodThis 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.
Target AreaThis 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.
Regulation DescriptionPercutaneous, Implanted, Long-term Intravascular Catheter.
Regulation Medical SpecialtyGeneral Hospital
Review PanelGeneral Hospital
Premarket Review Office Of Device Evaluation (ODE)
Division Of Anesthesiology, General Hospital, Infection Control, And Dental Devices (DAGRID)
General Hospital Devices Branch (GHDB)
Submission TypeEnforcement Discretion
CFR Regulation Number880.5970 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodePWR
GMP ExemptNo
Summary MRIneligible
Implanted DeviceNo
Life Support DeviceNo
Third Party Review Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

Device Type ID2767
DeviceCatheter Repair Kit
Product CodePWR
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionPercutaneous, Implanted, Long-term Intravascular Catheter.
CFR Regulation Number880.5970 [🔎]
Device Problems
Leak / Splash
1
Total Device Problems 1
TPLC Last Update: 2019-04-02 20:18:31

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.