ARISTOSURG 250— 510(k) K800395
Substantially EquivalentHalmon-Locren, Inc.
FDA 510(k) clearance K800395 for ARISTOSURG 250, Substantially Equivalent on 1980-03-17. Applicant: Halmon-Locren, Inc.. Device class: 1.
Clearance details
- Applicant
- Halmon-Locren, Inc.
- Product code
- Code EIA
- Device class
- Class 1
- Regulation
- 21 CFR 872.6640
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code EIA
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