Co2 Laser System, Models: PureLase And VanLase— 510(k) K232133
Substantially EquivalentCpmt Laser (Canadian Pioneer Medical Technology Corporation)
FDA 510(k) clearance K232133 for Co2 Laser System, Models: PureLase And VanLase, Substantially Equivalent on 2024-04-16. Applicant: Cpmt Laser (Canadian Pioneer Medical Technology Corporation). Device class: 2.
Clearance details
- Applicant
- Cpmt Laser (Canadian Pioneer Medical Technology Corporation)
- Product code
- Product code GEX
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Toronto, CA
Recent devices under product code GEX
view allMore clearances from Cpmt Laser (Canadian Pioneer Medical Technology Corporation)
view allAdverse events under product code GEX
product code GEX- Death
- 33
- Injury
- 3,045
- Malfunction
- 12,903
- Other
- 25
- Total
- 16,006
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.