# Sterilizer, Endodontic Dry Heat
> **Product code: KOK** · Class III — High Risk (PMA approval required, life-sustaining) · Dental · 21 CFR 872.6730
## Classification
- **FDA Product Code:** KOK
- **Device class:** Class III — High Risk (PMA approval required, life-sustaining)
- **Regulation:** 21 CFR 872.6730
- **Review panel:** DE
- **Medical specialty:** Dental
- **Submission type:** 2
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

Call for PMAs on 4/21/97 per 62 FR 2902 on 1/21/97

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