# Administrations Sets With Neuraxial Connectors
> **Product code: PWH** · Class II — Moderate Risk (510(k) clearance required) · General Hospital · 21 CFR 880.5440
## Classification
- **FDA Product Code:** PWH
- **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

The connector for neuraxial applications is intended to facilitate ANSI/AAMI/ISO 80369-6:2016 compliant neuraxial  specific connections.

## Market data
- **Cleared 510(k) submissions:** 4
- **Registered establishments:** 7
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=PWH)
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