FDA 510(k)

Crosperio OTW

K 號：K160013 · 2016-04-29

決定日期2016-04-29

產品代碼LIT

諮詢委員會履歷

決定相當於

器材摘要

Crosperio OTW is the device name listed in this FDA 510(k) record. The listed applicant is KANEKA Corporation. It received FDA 510(k) clearance on 2016-04-29 under 510(k) number K160013. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Crosperio OTW?

Crosperio OTW is a medical device that received FDA 510(k) clearance on 2016-04-29. The listed applicant is KANEKA Corporation. The 510(k) number is K160013.

When did Crosperio OTW receive FDA 510(k) clearance?

Crosperio OTW received FDA 510(k) clearance on 2016-04-29, under 510(k) number K160013.

Who is the listed applicant for Crosperio OTW?

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

What is the FDA product code for Crosperio OTW?

The FDA product code for Crosperio OTW is LIT.

其他以 KANEKA Corporation 為申請人之記錄

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。

K172264OTW Takeru PTCA 擴張球囊心导管 K170941RX NC Takeru PTCA 擴張球囊心导管 K163372RX Takeru 機器人氣球擴張導管 K163479R2P Metacross RX K160004Crosstella OTW K152873Crosstella RX 機器擴張導管

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相關器械（代碼：LIT）

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。

K260416ZYLOX Hippo PTA 擴張球囊心导管Zylox Medtech Co., Ltd.K254212NC PTA 機械擴張導管Kossel Medtech (Suzhou) Co., Ltd.K260304WAVE PTA 機器人球囊心导管WAVE Medical AG K252512Armada™ 14 NC PTA 穿刺導管ABBOTT MEDICAL K251915Amethyst HP PTA OTW 0.035 腔管Natec Medical , Ltd.K250706Passeo-35 Xeo 周邊擴張導管；Passeo-18 周邊擴張導管；Passeo-14 周邊擴張導管；Oscar 周邊多功能導管系統；Pantera Pro 射穿性經皮冠狀動脈成形術導管；Pantera LEO 射穿性經皮冠狀動脈成形術（PTCA）導管Biotronik, Inc.

官方來源

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