GECHO
K号: K250120 · 2025-07-14
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器械摘要
GECHO is the device name listed in this FDA 510(k) record. The listed applicant is Narnar, LLC. It received FDA 510(k) clearance on 2025-07-14 under 510(k) number K250120. 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 GECHO?
GECHO is a medical device that received FDA 510(k) clearance on 2025-07-14. The listed applicant is Narnar, LLC. The 510(k) number is K250120.
When did GECHO receive FDA 510(k) clearance?
GECHO received FDA 510(k) clearance on 2025-07-14, under 510(k) number K250120.
Who is the listed applicant for GECHO?
The FDA 510(k) record lists Narnar, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GECHO?
The FDA product code for GECHO is LLZ.
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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
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