# Sunlamp Products (Pre-Standard)
> **Product code: RAB** · Class II — Moderate Risk (510(k) clearance required) · General, Plastic Surgery · 21 CFR 878.4635
## Classification
- **FDA Product Code:** RAB
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 878.4635
- **Review panel:** SU
- **Medical specialty:** General, Plastic Surgery
- **Submission type:** 1
- **GMP exempt:** Y
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** Y
## Definition

A sunlamp product assembled or manufactured before november 9, 1979.  These are Class II medical devices as of 2014.

## Market data
- **Cleared 510(k) submissions:** 0
- **Registered establishments:** 2
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=RAB)
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