ICON 35; ICON 45; ICON 60; ICON 30FAF
K-번호: K260849 · 2026-06-11
광고
기기 요약
ICON 35; ICON 45; ICON 60; ICON 30FAF is the device name listed in this FDA 510(k) record. The listed applicant is Rehasense USA, Inc.. It received FDA 510(k) clearance on 2026-06-11 under 510(k) number K260849. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
자주 묻는 질문
What is the ICON 35; ICON 45; ICON 60; ICON 30FAF?
ICON 35; ICON 45; ICON 60; ICON 30FAF is a medical device that received FDA 510(k) clearance on 2026-06-11. The listed applicant is Rehasense USA, Inc.. The 510(k) number is K260849.
When did ICON 35; ICON 45; ICON 60; ICON 30FAF receive FDA 510(k) clearance?
ICON 35; ICON 45; ICON 60; ICON 30FAF received FDA 510(k) clearance on 2026-06-11, under 510(k) number K260849.
Who is the listed applicant for ICON 35; ICON 45; ICON 60; ICON 30FAF?
The FDA 510(k) record lists Rehasense USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ICON 35; ICON 45; ICON 60; ICON 30FAF?
The FDA product code for ICON 35; ICON 45; ICON 60; ICON 30FAF is IOR.
관련 기기 (코드: IOR)
관련 기록은 이름, 제품 코드 또는 기타 메타데이터를 사용하여 자동으로 매칭됩니다. 매칭은 검증된 임상, 과학, 기업 또는 규제 상의 관계를 입증하지 않으며, 연결된 공식 출처를 검토하시기 바랍니다.
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공식 출처
FDA 데이터베이스에서 보기 →FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.
광고