K172690 is the FDA 510(k) clearance record for ToFscan, a class II device, cleared for Idmed on 2018-05-31 under FDA product code KOI (Stimulator, Nerve, Peripheral, Electric). FDA records list 3 510(k) clearances for Idmed, from 2018-05-31 to 2025-08-12 . As of 2026-09-10 , FDA records show no recalls naming K172690.
Clearance record Decision date 2018-05-31 Received 2017-09-06 (267 days to decision) Product code KOI Stimulator, Nerve, Peripheral, ElectricRegulation 21 CFR 868.2775 Device class Class II Review panel Anesthesiology Applicant Idmed Hotel Technoptic - 2 Rue Marc Donadille, Marseille, FR 510(k) summary Summary PDF ↗ Third party review No
Clearances, product code KOI Trailing 12 months 1 clearance under product code KOI in the twelve months to October 2026, May 2026 the highest month at 1. Show the numbers FIRST ARTICLE / WEEKLY
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About this record Sourced from the FDA 510(k) premarket notification database, ingested from openFDA. MDM adds the decision time in days, the product code cross-link, recalls sharing that product code, and MDM coverage of the record.
Predicate devices are not listed. The openFDA 510(k) endpoint does not publish predicate references, so MDM does not assert them. Where a 510(k) summary exists, the FDA PDF is linked above and names the predicate itself.
Data as of 2026-09-28 , the FDA export date for this dataset. Page last changed 2026-09-05 . View this record on fda.gov ↗ (opens on fda.gov)
