EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System (K243793)
Description
EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System by Philips Ultrasound, LLC, an FDA 510(k) cleared radiology device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243793
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. EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System (K243793) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K240850 | EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series ... | Philips Ultrasound, LLC | 2024 |
Trace the full predicate network for K243793
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.