FDA 510(k)

M3290B 필립스 인텔루이브 정보 센터 iX

K-번호: K153702 · 2016-06-13

결정일2016-06-13

제품 코드MHX

자문 위원회CV

결정Substantially Equivalent

기기 요약

M3290B Philips IntelliVue Information Center iX is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2016-06-13 under 510(k) number K153702. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the M3290B Philips IntelliVue Information Center iX?

M3290B Philips IntelliVue Information Center iX is a medical device that received FDA 510(k) clearance on 2016-06-13. The listed applicant is Philips Medical Systems. The 510(k) number is K153702.

When did M3290B Philips IntelliVue Information Center iX receive FDA 510(k) clearance?

M3290B Philips IntelliVue Information Center iX received FDA 510(k) clearance on 2016-06-13, under 510(k) number K153702.

Who is the listed applicant for M3290B Philips IntelliVue Information Center iX?

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 M3290B Philips IntelliVue Information Center iX?

The FDA product code for M3290B Philips IntelliVue Information Center iX is MHX.

Philips Medical Systems를 신청인으로 등재한 기타 기록

K212704Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System K211597EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System K210560Page Writer TC20 Cardiograph, Page Writer TC30 Cardiograph, Page Writer TC50 Cardiograph, Page Writer TC70 Cardiograph K191738PageWriter TC20 Cardiograph, PageWriter TC30 Cardiograph, PageWriter TC50 Cardiograph, PageWriter TC70 Cardiograph K192875Philips Biosensor BX100 K183387M3290B Patient Information Center iX

14개 장치 모두 보기 →

공식 출처

FDA 데이터베이스에서 보기 →

FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.