Device |
cap, device disinfectant |
Regulation Description |
Intravascular administration set. |
Definition |
Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time |
Physical State |
A molded cap with a disinfectant pad to fit on a luer access device |
Technical Method |
Fits on a Luer Access Valve to disinfect the valve, then act as physical barrier to contamination |
Target Area |
Intravascular |
Regulation Medical Specialty |
General Hospital |
Review Panel |
General Hospital |
Product Code | QBP |
Premarket Review |
Office of Gastrorenal, ObGyn, General Hospital, and Urology Devices
(OHT3)
Drug Delivery and General Hospital Devices, and Human Factors
(DHT3C)
|
Submission Type |
510(k)
|
Regulation Number |
880.5440
|
Device Class |
2
|
Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
GMP Exempt? |
No
|
Summary Malfunction Reporting |
Ineligible |
Implanted Device? |
No
|
Life-Sustain/Support Device? |
No
|
Third Party Review |
Not Third Party Eligible |
|
|