LIGHTCAST II CARBIDE BLADE— 510(k) K760605
Substantially EquivalentMerck, Sharp & Dohme
FDA 510(k) clearance K760605 for LIGHTCAST II CARBIDE BLADE, Substantially Equivalent on 1976-10-05. Applicant: Merck, Sharp & Dohme.
Clearance details
- Applicant
- Merck, Sharp & Dohme
- Product code
- Code GES
- Advisory panel
- General, Plastic Surgery
- 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.