K250887
- 510(k) number
- K250887
- Device name
- Neuromuscular Transmission Monitor TOF3D (2510091)
- Applicant
- MIPM Mammendorfer Institut für Physik und Medizin GmbH DE
- Product code
- KOI — Stimulator, Nerve, Peripheral, Electric
- Decision date
- 2025-10-21
- Date received
- 2025-03-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K250887.pdf
Official FDA record: K250887
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.