Class Class U
Sonopet 1Q 3 7cm 1Q Large (K223770)
Description
Sonopet 1Q 3 7cm 1Q Large by Stryker Corporation, an FDA 510(k) cleared unknown device.
Regulatory Information
Device ClassClass Class U
510(k) NumberK223770
Clearance Date2023-02-16
Clearance TypeTraditional
Product CodeLFL
FDA Database
View on FDA DatabasePredicate lineage for K223770
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. Sonopet 1Q 3 7cm 1Q Large (K223770) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K213824 | Sonopet iQ Ultrasonic Aspirator System | Stryker Corporation | 2022 |
Trace the full predicate network for K223770
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.