RIESS-LUHR— 510(k) K811113
Substantially EquivalentAllomedic
FDA 510(k) clearance K811113 for RIESS-LUHR, Substantially Equivalent on 1981-06-16. Applicant: Allomedic. Device class: 1.
Clearance details
- Applicant
- Allomedic
- Product code
- Code DZA
- Device class
- Class 1
- Regulation
- 21 CFR 872.4130
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code DZA
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