Class Class II
Ascent Cardiorespiratory Diagnostic Software (K242809)
Description
Ascent Cardiorespiratory Diagnostic Software by Medical Graphics Corporation, an FDA 510(k) cleared anesthesiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242809
Clearance Date2024-10-17
Clearance TypeTraditional
Product CodeBTY
Regulation Number868.1890
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242809
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. Ascent Cardiorespiratory Diagnostic Software (K242809) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K181912 | Ascent Cardiorespiratory Diagnostic Software | Medical Graphics Corporation | 2019 |
| K133925 | VYNTUS/ SENTRYSUITE PRODUCT LINE | Carefusion Germany 234 GmbH | 2014 |
Trace the full predicate network for K242809
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.