FDA 510(k)

televere podiatry x-ray system hf

K-번호: K180765 · 2018-04-20

결정일2018-04-20

제품 코드KPR

자문 위원회[원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

결정대체적으로 동일

기기 요약

Televere Podiatry X-Ray System HF is the device name listed in this FDA 510(k) record. The listed applicant is Televere Systems, Inc.. It received FDA 510(k) clearance on 2018-04-20 under 510(k) number K180765. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Televere Podiatry X-Ray System HF?

Televere Podiatry X-Ray System HF is a medical device that received FDA 510(k) clearance on 2018-04-20. The listed applicant is Televere Systems, Inc.. The 510(k) number is K180765.

When did Televere Podiatry X-Ray System HF receive FDA 510(k) clearance?

Televere Podiatry X-Ray System HF received FDA 510(k) clearance on 2018-04-20, under 510(k) number K180765.

Who is the listed applicant for Televere Podiatry X-Ray System HF?

The FDA 510(k) record lists Televere Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Televere Podiatry X-Ray System HF?

The FDA product code for Televere Podiatry X-Ray System HF is KPR.

Televere Systems, Inc.를 신청인으로 등재한 기타 기록

K181358televere 디지털 치아 영상 시스템

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