G-2 VERSION 3, MODEL 10049— 510(k) K021890
Substantially EquivalentVitrolife Sweden AB
FDA 510(k) clearance K021890 for G-2 VERSION 3, MODEL 10049, Substantially Equivalent on 2002-09-06. Applicant: Vitrolife Sweden AB.
Clearance details
- Applicant
- Vitrolife Sweden AB
- Product code
- Code MQL
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.