# Peripheral Blood Processing Device For Wound Management
> **Product code: PMQ** · Class II — Moderate Risk (510(k) clearance required) · Hematology · 21 CFR 864.9245
## Classification
- **FDA Product Code:** PMQ
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 864.9245
- **Review panel:** HE
- **Medical specialty:** Hematology
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

Preparation of autologous platelet rich plasma gel from a small sample of peripheral blood for wound management.

## Market data
- **Cleared 510(k) submissions:** 0
- **Registered establishments:** 9
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=PMQ)
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