FDA 510(k)

D-Actor 200振动按摩系统

K号: K173692 · 2018-04-13

决定日期2018-04-13

产品代码ISA

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决定实质等同

器械摘要

D-Actor 200 Vibration Massage System is the device name listed in this FDA 510(k) record. The listed applicant is Storz Medical AG. It received FDA 510(k) clearance on 2018-04-13 under 510(k) number K173692. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the D-Actor 200 Vibration Massage System?

D-Actor 200 Vibration Massage System is a medical device that received FDA 510(k) clearance on 2018-04-13. The listed applicant is Storz Medical AG. The 510(k) number is K173692.

When did D-Actor 200 Vibration Massage System receive FDA 510(k) clearance?

D-Actor 200 Vibration Massage System received FDA 510(k) clearance on 2018-04-13, under 510(k) number K173692.

Who is the listed applicant for D-Actor 200 Vibration Massage System?

The FDA 510(k) record lists Storz Medical AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for D-Actor 200 Vibration Massage System?

The FDA product code for D-Actor 200 Vibration Massage System is ISA.

列明Storz Medical AG为申报人的其他记录

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

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