R&D PROJECT DW269#25— 510(k) K001469
Substantially EquivalentIvoclar North America, Inc.
FDA 510(k) clearance K001469 for R&D PROJECT DW269#25, Substantially Equivalent on 2000-07-05. Applicant: Ivoclar North America, Inc..
Clearance details
- Applicant
- Ivoclar North America, Inc.
- Product code
- Code EJS
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Amherst, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.