Atlas 振动调节仪器
K号: K172536 · 2018-06-20
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器械摘要
Atlas Percussion Adjusting Instrument is the device name listed in this FDA 510(k) record. The listed applicant is Spinalight, Inc.. It received FDA 510(k) clearance on 2018-06-20 under 510(k) number K172536. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.
常见问题
What is the Atlas Percussion Adjusting Instrument?
Atlas Percussion Adjusting Instrument is a medical device that received FDA 510(k) clearance on 2018-06-20. The listed applicant is Spinalight, Inc.. The 510(k) number is K172536.
When did Atlas Percussion Adjusting Instrument receive FDA 510(k) clearance?
Atlas Percussion Adjusting Instrument received FDA 510(k) clearance on 2018-06-20, under 510(k) number K172536.
Who is the listed applicant for Atlas Percussion Adjusting Instrument?
The FDA 510(k) record lists Spinalight, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Atlas Percussion Adjusting Instrument?
The FDA product code for Atlas Percussion Adjusting Instrument is LXM.
相关临床试验
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相关器械（代码：LXM）
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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