510(k) K110826
K110826 is an FDA 510(k) premarket notification submitted by Ivera Medical for the device "CUROS PORT PROTECTOR". The FDA issued a decision of Substantially Equivalent on June 23, 2011. The device falls under product code QBP (Cap, Device Disinfectant), a Class II device regulated under 21 CFR 880.5440. Ivera Medical has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 23, 2011
- Date Received
- March 24, 2011
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cap, Device Disinfectant
- Device Class
- Class II
- Regulation Number
- 880.5440
- Review Panel
- HO
- Submission Type
Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time