ASSISTO 通用夹持器
K号: K201279 · 2020-07-10
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器械摘要
ASSISTO Universal Applicator Clamping Device is the device name listed in this FDA 510(k) record. The listed applicant is Geomed Medizin-Technik GmbH & Co. KG. It received FDA 510(k) clearance on 2020-07-10 under 510(k) number K201279. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ASSISTO Universal Applicator Clamping Device?
ASSISTO Universal Applicator Clamping Device is a medical device that received FDA 510(k) clearance on 2020-07-10. The listed applicant is Geomed Medizin-Technik GmbH & Co. KG. The 510(k) number is K201279.
When did ASSISTO Universal Applicator Clamping Device receive FDA 510(k) clearance?
ASSISTO Universal Applicator Clamping Device received FDA 510(k) clearance on 2020-07-10, under 510(k) number K201279.
Who is the listed applicant for ASSISTO Universal Applicator Clamping Device?
The FDA 510(k) record lists Geomed Medizin-Technik GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASSISTO Universal Applicator Clamping Device?
The FDA product code for ASSISTO Universal Applicator Clamping Device is JAQ.
相关临床试验
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相关器械（代码：JAQ）
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。
官方来源
在 FDA 数据库中查看 →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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