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..
Clearance details
- Applicant
- Alexotek Co.
- Product code
- Code DZD
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.