K232543
- 510(k) number
- K232543
- Device name
- MSC SFM
- Applicant
- Yocon Biology Technology Company CN
- Product code
- NDS — Media, Culture, Ex Vivo, Tissue And Cell
- Decision date
- 2024-09-06
- Date received
- 2023-08-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232543.pdf
Official FDA record: K232543
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.