FDA 510(k)

Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V)

N.º K: K250701 · 2025-06-05

SolicitanteOlympus Medical Systems Corp.

Fecha de decisión2025-06-05

Código de productoFDT

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V) is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2025-06-05 under 510(k) number K250701. The device is classified under product code FDT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V)?

Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V) is a medical device that received FDA 510(k) clearance on 2025-06-05. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K250701.

When did Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V) receive FDA 510(k) clearance?

Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V) received FDA 510(k) clearance on 2025-06-05, under 510(k) number K250701.

Who is the listed applicant for Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V)?

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

What is the FDA product code for Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V)?

The FDA product code for Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V) is FDT.

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Otros registros que enlistan a Olympus Medical Systems Corp. como solicitante

K2620794K Camera Head OLYMPUS CH-S700-08-LB K254056THUNDERBEAT 5 mm, 45 cm, Tipo de Sujeción Actuada en la Frente S (TB-0545FCS); THUNDERBEAT 5 mm, 35 cm, Tipo de Sujeción Actuada en la Frente S (TB-0535FCS); THUNDERBEAT 5 mm, 20 cm, Tipo de Sujeción Actuada en la Frente S (TB-0520FCS)K260580Single Use Reloadable Clip Applicator (HX-810LR, HX-810UR); Clip (HX-610-090, HX-610-135); Long Clip (HX-610-090L, HX-610-135L); Short Clip (HX-610-090S, HX-610-135S); Super Short Clip (HX-610-135XS)K252341EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-Q190); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-H190 ); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-1TH190)K251807Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR K253646Single Use Distal Cover MAJ-2315 (MAJ-2315)

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Dispositivos relacionados (Código: FDT)

K251861FUJIFILM Endoscope Model ED-S100TP; FUJIFILM Endoscope Model ED-S100XP; FUJIFILM Processor Model VS-1000Fujifilm Corporation K253646Single Use Distal Cover MAJ-2315 (MAJ-2315)Olympus Medical Systems Corp.K251867EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V (TJF-Q190V)Olympus Medical Systems Corp.K233942PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical Video Processor (EPK-i8020c); PENTAX Medical Single Use, Sterile Distal End Cap with Elevator (OE-A63); Gas/Water Feeding Valves (OF-B194 )Pentax of America, Inc.K233886Ambu® aScope™ Duodeno 2, Ambu® aBox™ 2Ambu A/S K220587Evis Exera III Duodenovideoscope Olympus TJF-Q190VOlympus Medical Systems Corp.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.