PALADON ULTRA POWDER (PINK), PALADON ULTRA LIQUID— 510(k) K111832
Substantially EquivalentHeraeus Kulzer, LLC
FDA 510(k) clearance K111832 for PALADON ULTRA POWDER (PINK), PALADON ULTRA LIQUID, Substantially Equivalent on 2011-09-29. Applicant: Heraeus Kulzer, LLC.
Clearance details
- Applicant
- Heraeus Kulzer, LLC
- Product code
- Code EBI
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- South Bend, IN, US
Adverse events under product code EBI
product code EBI- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.