EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System
K-Number: K250177 · 2025-04-10
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 2025-04-10. It is manufactured by Philips Ultrasound, LLC. The 510(k) number is K250177.
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 2025-04-10, under approval number K250177.
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.