CERADRILL— 510(k) K071352
Substantially EquivalentGebr. Brasseler GmbH & Co. KG
FDA 510(k) clearance K071352 for CERADRILL, Substantially Equivalent on 2007-06-29. Applicant: Gebr. Brasseler GmbH & Co. KG.
Clearance details
- Applicant
- Gebr. Brasseler GmbH & Co. KG
- Product code
- Code EJL
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lemgo, DE
Adverse events under product code EJL
product code EJL- 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.