FDA 510(k)

AccuPoint Electrode

K 號：K162459 · 2017-06-15

申請人Microprobes For Life Science, Inc. Dba Neuron

決定日期2017-06-15

產品代碼GZL

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

AccuPoint Electrode is the device name listed in this FDA 510(k) record. The listed applicant is Microprobes For Life Science, Inc. Dba Neuron. It received FDA 510(k) clearance on 2017-06-15 under 510(k) number K162459. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AccuPoint Electrode?

AccuPoint Electrode is a medical device that received FDA 510(k) clearance on 2017-06-15. The listed applicant is Microprobes For Life Science, Inc. Dba Neuron. The 510(k) number is K162459.

When did AccuPoint Electrode receive FDA 510(k) clearance?

AccuPoint Electrode received FDA 510(k) clearance on 2017-06-15, under 510(k) number K162459.

Who is the listed applicant for AccuPoint Electrode?

The FDA 510(k) record lists Microprobes For Life Science, Inc. Dba Neuron as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AccuPoint Electrode?

The FDA product code for AccuPoint Electrode is GZL.

相關器械（代碼：GZL）

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：GZL）

官方來源