PERMAFLEX PERMANENT SOFT DENTURE RELINER— 510(k) K925062
Substantially EquivalentProtech Professional Products, Inc.
FDA 510(k) clearance K925062 for PERMAFLEX PERMANENT SOFT DENTURE RELINER, Substantially Equivalent on 1993-03-31. Applicant: Protech Professional Products, Inc..
Clearance details
- Applicant
- Protech Professional Products, Inc.
- Product code
- Code EBI
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Centereach, 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.