PLASTICEPH— 510(k) K810538
Substantially EquivalentMorningstar Dental Co.
FDA 510(k) clearance K810538 for PLASTICEPH, Substantially Equivalent on 1981-04-29. Applicant: Morningstar Dental Co.. Device class: 2.
Clearance details
- Applicant
- Morningstar Dental Co.
- Product code
- Code EAG
- Device class
- Class 2
- Regulation
- 21 CFR 872.1830
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code EAG
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