LuMon(TM) System— 510(k) K243765
Substantially EquivalentSentec AG
FDA 510(k) clearance K243765 for LuMon(TM) System, Substantially Equivalent on 2025-08-07. Applicant: Sentec AG. Device class: 2.
Clearance details
- Applicant
- Sentec AG
- Product code
- Code QEB
- Device class
- Class 2
- Regulation
- 21 CFR 868.1505
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Therwil, CH
Recent devices under product code QEB
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Data sourced from openFDA. This site is unofficial and independent of the FDA.