PERTAC-HYBRID— 510(k) K900510
Substantially EquivalentEspe GmbH (Us)
FDA 510(k) clearance K900510 for PERTAC-HYBRID, Substantially Equivalent on 1990-08-09. Applicant: Espe GmbH (Us).
Clearance details
- Applicant
- Espe GmbH (Us)
- Product code
- Code EBF
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Worth, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.