K240247
- 510(k) number
- K240247
- Device name
- MoFi Cell Culture Basal Medium
- Applicant
- Duogenic Stemcells Corporation TW
- Product code
- NDS — Media, Culture, Ex Vivo, Tissue And Cell
- Decision date
- 2024-07-12
- Date received
- 2024-01-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 1.5 MB · U.S. public domain
Also available from FDA: K240247.pdf
Official FDA record: K240247
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.