VINT
K号: K240385 · 2024-10-15
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器械摘要
VINT is the device name listed in this FDA 510(k) record. The listed applicant is Mediimg Corporation. It received FDA 510(k) clearance on 2024-10-15 under 510(k) number K240385. 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 VINT?
VINT is a medical device that received FDA 510(k) clearance on 2024-10-15. The listed applicant is Mediimg Corporation. The 510(k) number is K240385.
When did VINT receive FDA 510(k) clearance?
VINT received FDA 510(k) clearance on 2024-10-15, under 510(k) number K240385.
Who is the listed applicant for VINT?
The FDA 510(k) record lists Mediimg Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINT?
The FDA product code for VINT is LLZ.
相关器械（代码：LLZ）
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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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