Planmeca ProMax 3D Max, Planmeca Maximity
K号: K160506 · 2016-05-20
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器械摘要
Planmeca ProMax 3D Max, Planmeca Maximity is the device name listed in this FDA 510(k) record. The listed applicant is Planmeca Oy. It received FDA 510(k) clearance on 2016-05-20 under 510(k) number K160506. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Planmeca ProMax 3D Max, Planmeca Maximity?
Planmeca ProMax 3D Max, Planmeca Maximity is a medical device that received FDA 510(k) clearance on 2016-05-20. The listed applicant is Planmeca Oy. The 510(k) number is K160506.
When did Planmeca ProMax 3D Max, Planmeca Maximity receive FDA 510(k) clearance?
Planmeca ProMax 3D Max, Planmeca Maximity received FDA 510(k) clearance on 2016-05-20, under 510(k) number K160506.
Who is the listed applicant for Planmeca ProMax 3D Max, Planmeca Maximity?
The FDA 510(k) record lists Planmeca Oy as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Planmeca ProMax 3D Max, Planmeca Maximity?
The FDA product code for Planmeca ProMax 3D Max, Planmeca Maximity is OAS.
相关临床试验
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列明Planmeca Oy为申报人的其他记录
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相关器械（代码：OAS）
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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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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