AD POST— 510(k) K884277
Substantially EquivalentJ. Morita USA, Inc.
FDA 510(k) clearance K884277 for AD POST, Substantially Equivalent on 1988-12-22. Applicant: J. Morita USA, Inc.. Device class: 1.
Clearance details
- Applicant
- J. Morita USA, Inc.
- Product code
- Code ELR
- Device class
- Class 1
- Regulation
- 21 CFR 872.3810
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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