Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System
K-Number: K212704 · 2021-09-24
Device Summary
Frequently Asked Questions
What is the Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System?
Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2021-09-24. The listed applicant is Philips Medical Systems. The 510(k) number is K212704.
When did Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System receive FDA 510(k) clearance?
Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System received FDA 510(k) clearance on 2021-09-24, under 510(k) number K212704.
Who is the listed applicant for Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System?
The FDA 510(k) record lists Philips Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System?
The FDA product code for Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System is IYN.
Other records listing Philips Medical Systems as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IYN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.