MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE— 510(k) K871934
Substantially EquivalentLasermatic, Inc.
FDA 510(k) clearance K871934 for MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE, Substantially Equivalent on 1988-03-25. Applicant: Lasermatic, Inc..
Clearance details
- Applicant
- Lasermatic, Inc.
- Product code
- Code LNK
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dallas, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.