INFIBRA, MODEL 1200— 510(k) K061735
Substantially EquivalentGlobal Dental Products, Inc.
FDA 510(k) clearance K061735 for INFIBRA, MODEL 1200, Substantially Equivalent on 2006-09-08. Applicant: Global Dental Products, Inc..
Clearance details
- Applicant
- Global Dental Products, Inc.
- Product code
- Code EBI
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wantagh, NY, 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.