K233177
- 510(k) number
- K233177
- Device name
- Nest VT Vitrification Device
- Applicant
- Cook Incorporated IN · US
- Product code
- MQK — Labware, Assisted Reproduction
- Decision date
- 2024-03-08
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233177.pdf
Official FDA record: K233177
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.