D2P
K号: K183489 · 2019-08-29
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器械摘要
D2P is the device name listed in this FDA 510(k) record. The listed applicant is 3D Systems, Inc.. It received FDA 510(k) clearance on 2019-08-29 under 510(k) number K183489. 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 D2P?
D2P is a medical device that received FDA 510(k) clearance on 2019-08-29. The listed applicant is 3D Systems, Inc.. The 510(k) number is K183489.
When did D2P receive FDA 510(k) clearance?
D2P received FDA 510(k) clearance on 2019-08-29, under 510(k) number K183489.
Who is the listed applicant for D2P?
The FDA 510(k) record lists 3D Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for D2P?
The FDA product code for D2P is LLZ.
列明3D Systems, 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。
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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