EmbryoScope+— 510(k) K173264
Substantially EquivalentVitrolife A/S
FDA 510(k) clearance K173264 for EmbryoScope+, Substantially Equivalent on 2018-05-11. Applicant: Vitrolife A/S. Device class: 2.
Clearance details
- Applicant
- Vitrolife A/S
- Product code
- Code MQG
- Device class
- Class 2
- Regulation
- 21 CFR 884.6120
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Viby J, DK
Recent devices under product code MQG
view all- K261083 — Wallace® Aspiration Pump (WAPV1); Wallace® Pump Filter Connector (WFC); Wallace® Vacuum Connection Kit (WVCK)
- K260194 — Vacuum Pump (Model: AD-VPUM-500)
- K242684 — Harioculture TL-16 Time-lapse Incubator
- K232493 — Embryo Real-time Incubator (TLS301), Embryo Real-time Culture Dish (MC 2004)
- K180188 — Geri Embryo Incubator with Geri Connect and Geri Assess Software, and Geri Dish
More clearances from Vitrolife A/S
view allData sourced from openFDA. This site is unofficial and independent of the FDA.