# Uric Acid Test System For At Home Prescription Use
> **Product code: PTC** · Class I — Low Risk (general controls) · Clinical Chemistry · 21 CFR 862.1775
## Classification
- **FDA Product Code:** PTC
- **Device class:** Class I — Low Risk (general controls)
- **Regulation:** 21 CFR 862.1775
- **Review panel:** CH
- **Medical specialty:** Clinical Chemistry
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** Y
## Definition

For the quantitative measurement of uric acid in home use settings by patients diagnosed with gout. This device is for prescription use only.

## Market data
- **Cleared 510(k) submissions:** 3
- **Registered establishments:** 5
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=PTC)
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