Product Classification

• Device: catheter, intravascular, therapeutic, long-term greater than 30 days
• Regulation Description: Percutaneous, implanted, long-term intravascular catheter.
• Regulation Medical Specialty: General Hospital
• Review Panel: General Hospital
• Product Code: LJS
• Premarket Review: Drug Delivery and General Hospital Devices, and Human Factors (DHT3C); Drug Delivery and General Hospital Devices, and Human Factors (DHT3C)
• Submission Type: 510(k)
• Regulation Number: 880.5970
• Device Class: 2
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No
• Summary Malfunction Reporting: Eligible
• Implanted Device?: Yes
• Life-Sustain/Support Device?: No

Recognized Consensus Standards

• 3-176 ISO 18193 First edition 2021-08
  Cardiovascular implants and artificial organs - Cannulae for extracorporeal circulation
• 3-183 ISO 11658 First edition 2012-05-15
  Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems
• 6-273 ISO 23908 First edition 2011-06-11
  Sharps injury protection - Requirements and test methods - Sharps protection features for single-use hypodermic needles, introducers for catheters and needles used for blood sampling
• 6-305 ISO 10555-3 Second edition 2013-06-15
  Intravascular catheters -- Sterile and single-use catheters -- Part 3: Central venous catheters
• 6-408 ISO 10555-1 Second edition 2013-06-15
  Intravascular catheters - Sterile and single-use intravascular catheters - Part 1: General requirements [Including AMENDMENT 1 (2017)]
• 6-499 ISO 10555-1 Third edition 2023-11
  Intravascular catheters - Sterile and single-use intravascular catheters - Part 1: General requirements

Guidance Documents

• Intravascular Catheters, Wires, and Delivery Systems with Lubricious Coatings - Labeling Considerations: Guidance for Industry and Food and Drug Administration Staff

• Guidance on Premarket Notification [510(K)] Submissions for Short-Term and Long-Term Intravascular Catheters

Third Party Review

Not Third Party Eligible