EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System
K-Number: K253595 · 2026-03-27
Device Summary
Frequently Asked Questions
What is the EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System?
EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2026-03-27. It is manufactured by Philips Ultrasound, LLC. The 510(k) number is K253595.
When was EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System approved by the FDA?
EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System received FDA 510(k) clearance on 2026-03-27, under approval number K253595.
What company makes EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System?
EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System is manufactured by Philips Ultrasound, LLC.
What is the FDA product code for EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System?
The FDA product code for EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System is IYN.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.