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FDA 510(k)

Terragene® Bionova® Photon 带独特点集成器的工艺挑战设备 (PCD225-2);Terragene® Bionova® Photon 带移动前沿集成器的工艺挑战设备 (PCD225-C)

K号: K242453 · 2024-12-12

申请人Terragene S.A.
决定日期2024-12-12
产品代码FRC
咨询委员会医疗设备监管文本翻译如下： HO 请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C) is the device name listed in this FDA 510(k) record. The listed applicant is Terragene S.A.. It received FDA 510(k) clearance on 2024-12-12 under 510(k) number K242453. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C)?

Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C) is a medical device that received FDA 510(k) clearance on 2024-12-12. The listed applicant is Terragene S.A.. The 510(k) number is K242453.

When did Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C) receive FDA 510(k) clearance?

Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C) received FDA 510(k) clearance on 2024-12-12, under 510(k) number K242453.

Who is the listed applicant for Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C)?

The FDA 510(k) record lists Terragene S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C)?

The FDA product code for Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C) is FRC.

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Terragene S.A.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。

K231383Terragene® Bionova® 自包含生物指示器 (BT95), Terragene® Bionova® 自包含生物指示器 (BT96), Terragene® Chemdye® 化学工艺指示器 (CD42), Terragene® Cintape® 化学工艺指示器胶带 (CT40)K232103Terragene® Chemdye® 多变量化学指示器 (CD40), Terragene® Chemdye® 化学工艺指示器 (CD42), Terragene® Cintape® 化学工艺指示器胶带 (CT40)K221641Terragene® Bionova® Hyper 生物指示器 (BT98), Terragene® Bionova® Hyper 自动读取孵育箱 (BHY), Terragene® Bionova® NanoBio 自动读取孵育箱 (BNB)K200272Terragene ChemdyeK191021Terragene Bionova, Terragene Bionova, Terragene Integron, Terragene Cintape, Terragene ChemdyeK163646Terragene Bionova(R) SCBI (BT220, BT221, BT222, BT223), Terragene Bionova (R) PCD (PCD220-C, PCD220-2, PCD222-C, PCD222-2), 以及 Terragene Bionova(R) IC10/20FR 读取孵育箱

查看所有 7 个设备 →

相关器械（代码：FRC）

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。

K260766Celerity 5 HP 生物指示剂（LCB052）STERIS CorporationK252680Celerity™ 20 HP 生物指示剂STERIS CorporationK251122Terragene® Bionova® BT20 生物指示器TerrageneK251452Celerity 5 HP 生物指示剂（LCB052）；Celerity 5 HP 挑战包（LCB059）；Celerity 20 HP 生物指示剂（LCB044）；Celerity 20 HP 挑战包（LCB045）SterisK250044Celerity 5 HP 生物指示剂（LCB052）；Celerity 5 HP 挑战包（LCB059）；Celerity 20 HP 生物指示剂（LCB044）；Celerity 20 HP 挑战包（LCB045）STERIS CorporationK250061Celerity 孵化箱STERIS Corporation

官方来源

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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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