THE DIRECTION DIAL— 510(k) K882309
Substantially EquivalentLawhorn Innovations
FDA 510(k) clearance K882309 for THE DIRECTION DIAL, Substantially Equivalent on 1988-06-23. Applicant: Lawhorn Innovations. Device class: 1.
Clearance details
- Applicant
- Lawhorn Innovations
- Product code
- Code EKJ
- Device class
- Class 1
- Regulation
- 21 CFR 872.4565
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Missoula, MT, US
Recent devices under product code EKJ
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