FDA 510(k)

Single-Use Biopsy Valve (MAJ-1555)

Número K: K251997 · 2025-09-25

RequerenteOlympus Medical Systems Corporation

Data da decisão2025-09-25

Código do produtoOCX

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Single-Use Biopsy Valve (MAJ-1555) is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corporation. It received FDA 510(k) clearance on 2025-09-25 under 510(k) number K251997. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Single-Use Biopsy Valve (MAJ-1555)?

Single-Use Biopsy Valve (MAJ-1555) is a medical device that received FDA 510(k) clearance on 2025-09-25. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K251997.

When did Single-Use Biopsy Valve (MAJ-1555) receive FDA 510(k) clearance?

Single-Use Biopsy Valve (MAJ-1555) received FDA 510(k) clearance on 2025-09-25, under 510(k) number K251997.

Who is the listed applicant for Single-Use Biopsy Valve (MAJ-1555)?

The FDA 510(k) record lists Olympus Medical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Single-Use Biopsy Valve (MAJ-1555)?

The FDA product code for Single-Use Biopsy Valve (MAJ-1555) is OCX.

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Outros registros que listam Olympus Medical Systems Corporation como candidato(a)

K260824Gastrointestinal Videoscope Olympus GIF-2T1500 K260856Disposable Distal Attachment D-201-13404 K260401EVIS EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE OLYMPUS BF-UCP190F (BF-UCP190F)K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)K261260HD Camera Head OLYMPUS CH-S200-08-LB K252050Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D

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Fonte oficial

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