K232405
- 510(k) number
- K232405
- Device name
- ENDOFIX EXO
- Applicant
- Aktormed GmbH DE
- Product code
- OCV — Endoscope Holder
- Decision date
- 2024-04-25
- Date received
- 2023-08-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K232405.pdf
Official FDA record: K232405
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.