LABIAL CUSPID TUBE— 510(k) K834392
Substantially EquivalentAlexotek Co.
FDA 510(k) clearance K834392 for LABIAL CUSPID TUBE, Substantially Equivalent on 1984-02-28. Applicant: Alexotek Co.. Device class: 1.
Clearance details
- Applicant
- Alexotek Co.
- Product code
- Code DZD
- Device class
- Class 1
- Regulation
- 21 CFR 872.5410
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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