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FDA 510(k)

PENTAX 医疗视频十二指肠镜 (ED34-i10T2s)；PENTAX 医疗视频处理器 (EPK-i8020c)；PENTAX 医疗一次性，无菌远端帽带提升器 (OE-A63)；气/水供应阀门 (OF-B194 )

K号: K233942 · 2024-08-01

申请人Pentax of America, Inc.
决定日期2024-08-01
产品代码FDT
咨询委员会GU 请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定实质等同

器械摘要

PENTAX 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 ) is the device name listed in this FDA 510(k) record. The listed applicant is Pentax of America, Inc.. It received FDA 510(k) clearance on 2024-08-01 under 510(k) number K233942. The device is classified under product code FDT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the PENTAX 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 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 ) is a medical device that received FDA 510(k) clearance on 2024-08-01. The listed applicant is Pentax of America, Inc.. The 510(k) number is K233942.

When did PENTAX 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 ) receive FDA 510(k) clearance?

PENTAX 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 ) received FDA 510(k) clearance on 2024-08-01, under 510(k) number K233942.

Who is the listed applicant for PENTAX 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 )?

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

What is the FDA product code for PENTAX 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 )?

The FDA product code for PENTAX 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 ) is FDT.

相关临床试验

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Pentax of America, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K251256PENTAX 医疗视频上消化道镜 (EG 系列) (EG 系列)；PENTAX 医疗视频结肠镜 (EC 系列) (EC 系列)K251127PENTAX 医疗视频处理器 (EPK-i8020c)K242110PENTAX 医疗视频结肠镜 (EC38-i20cWL)K241213PENTAX 医疗视频上消化道镜 (EG27-i20c)；PENTAX 医疗视频结肠镜 (EC34-i20cL)K240457C2 冷冻球囊消融系统（C2 冷冻球囊消融系统）K232860PENTAX 医疗视频处理器 EPK-i8020c，PENTAX 医疗视频支气管镜 EB11-J10，PENTAX 医疗视频支气管镜 EB15-J10，PENTAX 医疗视频支气管镜 EB19-J10U，PENTAX 医疗超声视频支气管镜 EB19-J10U

查看所有 39 个设备 →

相关器械（代码：FDT）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K251861富士胶片内窥镜型号ED-S100TP; 富士胶片内窥镜型号ED-S100XP; 富士胶片处理器型号VS-1000Fujifilm CorporationK253646一次性远端盖 MAJ-2315 (MAJ-2315)Olympus Medical Systems Corp.K251867EVIS EXERA III 十二指肠镜 OLYMPUS TJF-Q190V (TJF-Q190V)Olympus Medical Systems Corp.K250701Evis Exera III十二指肠内窥镜Olympus TJF-Q190V（TJF-Q190V）Olympus Medical Systems Corp.K233886Ambu® aScope™ Duodeno 2, Ambu® aBox™ 2Ambu A/SK220587Evis Exera III十二指肠内窥镜Olympus TJF-Q190VOlympus Medical Systems Corp.

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。

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