WiTOF— 510(k) K243339
Substantially EquivalentIdmed
FDA 510(k) clearance K243339 for WiTOF, Substantially Equivalent on 2025-06-23. Applicant: Idmed. Device class: 2.
Clearance details
- Applicant
- Idmed
- Product code
- Code KOI
- Device class
- Class 2
- Regulation
- 21 CFR 868.2775
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Marseille, FR
Recent devices under product code KOI
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- K242525 — iTOF®
- K220530 — Tetragraph Neuromuscular Transmission Monitor
- K220976 — Life Scope PT BSM-1700 Series Bedside Monitor
More clearances from Idmed
view allData sourced from openFDA. This site is unofficial and independent of the FDA.