FDA 510(k)

Alturion 시리즈 진단超음파 시스템

K-번호: K262311 · 2026-08-04

결정일2026-08-04

제품 코드IYN

자문 위원회RA

결정Substantially Equivalent

기기 요약

Alturion Series Diagnostic Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, LLC. It received FDA 510(k) clearance on 2026-08-04 under 510(k) number K262311. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Alturion Series Diagnostic Ultrasound System?

Alturion Series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2026-08-04. The listed applicant is Philips Ultrasound, LLC. The 510(k) number is K262311.

When did Alturion Series Diagnostic Ultrasound System receive FDA 510(k) clearance?

Alturion Series Diagnostic Ultrasound System received FDA 510(k) clearance on 2026-08-04, under 510(k) number K262311.

Who is the listed applicant for Alturion Series Diagnostic Ultrasound System?

The FDA 510(k) record lists Philips Ultrasound, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Alturion Series Diagnostic Ultrasound System?

The FDA product code for Alturion Series Diagnostic Ultrasound System is IYN.

Philips Ultrasound, LLC를 신청인으로 등재한 기타 기록

K262548EPIQ Inspira Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System K261211Philips EPIQ Series Diagnostic Ultrasound System; Philips Affiniti Series Diagnostic Ultrasound System K260667Alturion 시리즈 진단超음파 시스템 K260123EPIQ Series Diagnostic Ultrasound System K260680EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems K252558Lumify Diagnostic Ultrasound System

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