FDA 510(k)

See Factor CT3™

K-번호: K233230 · 2024-06-21

결정일2024-06-21

제품 코드OWB

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

결정대체적으로 동일

기기 요약

See Factor CT3™ is the device name listed in this FDA 510(k) record. The listed applicant is Epica International, Inc.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233230. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the See Factor CT3™?

See Factor CT3™ is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Epica International, Inc.. The 510(k) number is K233230.

When did See Factor CT3™ receive FDA 510(k) clearance?

See Factor CT3™ received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233230.

Who is the listed applicant for See Factor CT3™?

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

What is the FDA product code for See Factor CT3™?

The FDA product code for See Factor CT3™ is OWB.

Epica International, Inc.를 신청인으로 등재한 기타 기록

K190856SeeFactorCT3

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