MINIFLEX AND PERSONAL UNIT— 510(k) K912997
Substantially EquivalentDabi-Atlante America Corp.
FDA 510(k) clearance K912997 for MINIFLEX AND PERSONAL UNIT, Substantially Equivalent on 1991-10-30. Applicant: Dabi-Atlante America Corp.. Device class: 1.
Clearance details
- Applicant
- Dabi-Atlante America Corp.
- Product code
- Code EAZ
- Device class
- Class 1
- Regulation
- 21 CFR 872.4630
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tampa, FL, US
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