# Cap, Device Disinfectant
> **Product code: QBP** · Class II — Moderate Risk (510(k) clearance required) · General Hospital · 21 CFR 880.5440
## Classification
- **FDA Product Code:** QBP
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 880.5440
- **Review panel:** HO
- **Medical specialty:** General Hospital
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time

## Market data
- **Cleared 510(k) submissions:** 22
- **Registered establishments:** 30
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=QBP)
---
*AI Analytics · CC0 1.0*