RAPID-I— 510(k) K090832
Substantially EquivalentVitrolife Sweden AB
FDA 510(k) clearance K090832 for RAPID-I, Substantially Equivalent on 2009-12-23. Applicant: Vitrolife Sweden AB. Device class: 2.
Clearance details
- Applicant
- Vitrolife Sweden AB
- Product code
- Product code MQK
- Device class
- Class 2
- Regulation
- 21 CFR 884.6160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Se-400 92 Goteborg, SE
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