RAPIDVIT BLAST, RAPIDWARM BLAST— 510(k) K101003
Substantially EquivalentVitrolife Sweden AB
FDA 510(k) clearance K101003 for RAPIDVIT BLAST, RAPIDWARM BLAST, Substantially Equivalent on 2010-12-10. Applicant: Vitrolife Sweden AB. Device class: 2.
Clearance details
- Applicant
- Vitrolife Sweden AB
- Product code
- Code MQL
- Device class
- Class 2
- Regulation
- 21 CFR 884.6180
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Se-400 92 Goteborg, SE
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