FDA 510(k)

UniStrip1 通用血糖試紙

K 號：K162430 · 2017-01-19

決定日期2017-01-19

產品代碼NBW

諮詢委員會CH

決定相當於

器材摘要

UniStrip1 Generic Blood Glucose Test Strips is the device name listed in this FDA 510(k) record. The listed applicant is Ok Biotech Co., Ltd.. It received FDA 510(k) clearance on 2017-01-19 under 510(k) number K162430. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常見問題

What is the UniStrip1 Generic Blood Glucose Test Strips?

UniStrip1 Generic Blood Glucose Test Strips is a medical device that received FDA 510(k) clearance on 2017-01-19. The listed applicant is Ok Biotech Co., Ltd.. The 510(k) number is K162430.

When did UniStrip1 Generic Blood Glucose Test Strips receive FDA 510(k) clearance?

UniStrip1 Generic Blood Glucose Test Strips received FDA 510(k) clearance on 2017-01-19, under 510(k) number K162430.

Who is the listed applicant for UniStrip1 Generic Blood Glucose Test Strips?

The FDA 510(k) record lists Ok Biotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UniStrip1 Generic Blood Glucose Test Strips?

The FDA product code for UniStrip1 Generic Blood Glucose Test Strips is NBW. This falls under the OB/GYN category.

其他以 Ok Biotech Co., Ltd. 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。

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相關器械（代碼：NBW）

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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