HYBRID RESIN COMPOSITE— 510(k) K964867
Substantially EquivalentParkell, Inc.
FDA 510(k) clearance K964867 for HYBRID RESIN COMPOSITE, Substantially Equivalent on 1997-04-11. Applicant: Parkell, Inc..
Clearance details
- Applicant
- Parkell, Inc.
- Product code
- Code KLE
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Farmingdale, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.