Class Class II
Clearo (K242438)
Description
Clearo by Breas Medical AB, an FDA 510(k) cleared anesthesiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242438
Clearance Date2025-05-16
Clearance TypeTraditional
Product CodeNHJ
Regulation Number868.5905
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242438
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Clearo (K242438) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K191912 | BiWaze Cough | Abmrc, LLC | 2020 |
| K121955 | COUGHASSIST T70 DEVICE | Respironics, Inc. | 2012 |
Trace the full predicate network for K242438
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.