510(k) K123967
K123967 is an FDA 510(k) premarket notification submitted by Catheter Connections, Inc. for the device "CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS". The FDA issued a decision of Substantially Equivalent on January 22, 2013. The device falls under product code QBP (Cap, Device Disinfectant), a Class II device regulated under 21 CFR 880.5440. Catheter Connections, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 22, 2013
- Date Received
- December 26, 2012
- Clearance Type
- Special
- 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