火炬™ 软件
K号: K220630 · 2022-11-28
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器械摘要
TorchTM Software is the device name listed in this FDA 510(k) record. The listed applicant is Voximetry, Incorporated. It received FDA 510(k) clearance on 2022-11-28 under 510(k) number K220630. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the TorchTM Software?
TorchTM Software is a medical device that received FDA 510(k) clearance on 2022-11-28. The listed applicant is Voximetry, Incorporated. The 510(k) number is K220630.
When did TorchTM Software receive FDA 510(k) clearance?
TorchTM Software received FDA 510(k) clearance on 2022-11-28, under 510(k) number K220630.
Who is the listed applicant for TorchTM Software?
The FDA 510(k) record lists Voximetry, Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TorchTM Software?
The FDA product code for TorchTM Software is LLZ.
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相关器械（代码：LLZ）
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。
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请注意，由于您没有提供具体的医疗设备监管文本，我无法提供准确的翻译。如果您能提供具体的文本内容，我将能够为您提供准确的翻译。Taiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC
官方来源
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