PIEZON MASTER 400— 510(k) K896749
Substantially EquivalentElectro Medical Systems (Ems Sa)
FDA 510(k) clearance K896749 for PIEZON MASTER 400, Substantially Equivalent on 1990-08-31. Applicant: Electro Medical Systems (Ems Sa).
Clearance details
- Applicant
- Electro Medical Systems (Ems Sa)
- Product code
- Code ELC
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Nyon, CH
Adverse events under product code ELC
product code ELC- Malfunction
- 1,255
- Total
- 1,255
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.