# Stabilizer, Heart, Non-Compression, Reprocessed
> **Product code: NQG** · Class I — Low Risk (general controls) · Cardiovascular · 21 CFR 870.4500
## Classification
- **FDA Product Code:** NQG
- **Device class:** Class I — Low Risk (general controls)
- **Regulation:** 21 CFR 870.4500
- **Review panel:** CV
- **Medical specialty:** Cardiovascular
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** Y
## Definition

The device is used to stabilize, move, lift, and position the heart during cardiovascular surgery. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).

## Market data
- **Cleared 510(k) submissions:** 3
- **Registered establishments:** 1
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=NQG)
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