PROLITE PULSED LIGHT SYSTEM FOR THE REMOVAL OF UNWANTED HAIR— 510(k) K013366
Substantially EquivalentMedical Bio Care Sweden AB
FDA 510(k) clearance K013366 for PROLITE PULSED LIGHT SYSTEM FOR THE REMOVAL OF UNWANTED HAIR, Substantially Equivalent on 2002-01-08. Applicant: Medical Bio Care Sweden AB.
Clearance details
- Applicant
- Medical Bio Care Sweden AB
- Product code
- Code GEX
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Woodland, CA, US
Adverse 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.