K233764
- 510(k) number
- K233764
- Device name
- SSS-NX (Serum Substitute Supplement-NX)
- Applicant
- Fujifilm Irvine Scientific CA · US
- Product code
- MQL — Media, Reproductive
- Decision date
- 2024-04-24
- Date received
- 2023-11-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K233764.pdf
Official FDA record: K233764
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.