MW 8000-I— 510(k) K792303
Substantially EquivalentMidwest
FDA 510(k) clearance K792303 for MW 8000-I, Substantially Equivalent on 1979-11-27. Applicant: Midwest. Device class: 2.
Clearance details
- Applicant
- Midwest
- Product code
- Code EBF
- Device class
- Class 2
- Regulation
- 21 CFR 872.3690
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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