FDA 510(k)

어ーリ포인트 평가

K-번호: K253442 · 2026-03-05

결정일2026-03-05

제품 코드QPF

자문 위원회NE (이 문서는 원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.)

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기기 요약

EarliPoint Assessment is the device name listed in this FDA 510(k) record. The listed applicant is Earlitec Diagnostics. It received FDA 510(k) clearance on 2026-03-05 under 510(k) number K253442. The device is classified under product code QPF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the EarliPoint Assessment?

EarliPoint Assessment is a medical device that received FDA 510(k) clearance on 2026-03-05. The listed applicant is Earlitec Diagnostics. The 510(k) number is K253442.

When did EarliPoint Assessment receive FDA 510(k) clearance?

EarliPoint Assessment received FDA 510(k) clearance on 2026-03-05, under 510(k) number K253442.

Who is the listed applicant for EarliPoint Assessment?

The FDA 510(k) record lists Earlitec Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EarliPoint Assessment?

The FDA product code for EarliPoint Assessment is QPF.

Earlitec Diagnostics를 신청인으로 등재한 기타 기록

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