FDA 510(k)

Atellica CH 苯环己哌啶（Pcp）

K号: K163220 · 2017-04-06

决定日期2017-04-06

产品代码LCM

决定实质等同

器械摘要

Atellica CH Phencyclidine (Pcp) is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare Diagnostics, Inc.. It received FDA 510(k) clearance on 2017-04-06 under 510(k) number K163220. The device is classified under product code LCM. FDA Decision: Substantially Equivalent.

常见问题

What is the Atellica CH Phencyclidine (Pcp)?

Atellica CH Phencyclidine (Pcp) is a medical device that received FDA 510(k) clearance on 2017-04-06. The listed applicant is Siemens Healthcare Diagnostics, Inc.. The 510(k) number is K163220.

When did Atellica CH Phencyclidine (Pcp) receive FDA 510(k) clearance?

Atellica CH Phencyclidine (Pcp) received FDA 510(k) clearance on 2017-04-06, under 510(k) number K163220.

Who is the listed applicant for Atellica CH Phencyclidine (Pcp)?

FDA 510(k)记录中列出西门子医疗诊断公司（Siemens Healthcare Diagnostics, Inc.）为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for Atellica CH Phencyclidine (Pcp)?

The FDA product code for Atellica CH Phencyclidine (Pcp) is LCM.

列明Siemens Healthcare Diagnostics, Inc.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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