LIGHT-TOUCH/GS 905250 ND:YAG LASER MICRO PRO ENDOS— 510(k) K891909
Substantially EquivalentLifestream Int'L, Inc.
FDA 510(k) clearance K891909 for LIGHT-TOUCH/GS 905250 ND:YAG LASER MICRO PRO ENDOS, Substantially Equivalent on 1989-05-26. Applicant: Lifestream Int'L, Inc..
Clearance details
- Applicant
- Lifestream Int'L, Inc.
- Product code
- Code GEX
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- The Woodlands, TX, 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.