Class Class II
STS (K240293)
Description
STS by Techbopulm, Ltd., an FDA 510(k) cleared anesthesiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240293
Clearance Date2024-09-17
Clearance TypeTraditional
Product CodeBZC
Regulation Number868.1880
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240293
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. STS (K240293) cites 4 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K161295 | MiniBox + | Pulmone Advanced Medical Devices, Ltd. | 2016 |
| K152585 | Resmon PRO FULL | Medical Graphics Corp. | 2016 |
| K111408 | MICROGARD II | Carefusion Germany 234 GmbH | 2011 |
| K051712 | MODEL 2800 PFT FILTER | Air Safety, Ltd. | 2005 |
Trace the full predicate network for K240293
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.