K241897
- 510(k) number
- K241897
- Device name
- MOR
- Applicant
- Morari, Inc. MN · US
- Product code
- QRC — Non-Implanted Electrical Stimulation Device For Mana
- Decision date
- 2025-02-11
- Date received
- 2024-06-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K241897.pdf
Official FDA record: K241897
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.