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FDA 510(k)

IPG，整合式，25/40公分，單針，鋸齒形，IPG，2公分，單針4，導線（25/40公分，4，鋸齒形），延伸線 - 4

K 號：K191435 · 2019-09-06

申請人Nalu Medical, Inc.
決定日期2019-09-06
產品代碼GZF
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

IPG, integrated, 25/40 cm, single, tined, IPG, 2 cm, single 4, Lead (25/40 cm, 4, tined), Extension - 4 is the device name listed in this FDA 510(k) record. The listed applicant is Nalu Medical, Inc.. It received FDA 510(k) clearance on 2019-09-06 under 510(k) number K191435. The device is classified under product code GZF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the IPG, integrated, 25/40 cm, single, tined, IPG, 2 cm, single 4, Lead (25/40 cm, 4, tined), Extension - 4?

IPG, integrated, 25/40 cm, single, tined, IPG, 2 cm, single 4, Lead (25/40 cm, 4, tined), Extension - 4 is a medical device that received FDA 510(k) clearance on 2019-09-06. The listed applicant is Nalu Medical, Inc.. The 510(k) number is K191435.

When did IPG, integrated, 25/40 cm, single, tined, IPG, 2 cm, single 4, Lead (25/40 cm, 4, tined), Extension - 4 receive FDA 510(k) clearance?

IPG, integrated, 25/40 cm, single, tined, IPG, 2 cm, single 4, Lead (25/40 cm, 4, tined), Extension - 4 received FDA 510(k) clearance on 2019-09-06, under 510(k) number K191435.

Who is the listed applicant for IPG, integrated, 25/40 cm, single, tined, IPG, 2 cm, single 4, Lead (25/40 cm, 4, tined), Extension - 4?

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

What is the FDA product code for IPG, integrated, 25/40 cm, single, tined, IPG, 2 cm, single 4, Lead (25/40 cm, 4, tined), Extension - 4?

The FDA product code for IPG, integrated, 25/40 cm, single, tined, IPG, 2 cm, single 4, Lead (25/40 cm, 4, tined), Extension - 4 is GZF.

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相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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