FDA 510(k)

氧適 pulse 氧氣濃度計

K 號：K203812 · 2022-11-08

決定日期2022-11-08

產品代碼DQA

諮詢委員會履歷

決定相當於

器材摘要

Oxyfit Pulse Oximeter is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Viatom Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-08 under 510(k) number K203812. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Oxyfit Pulse Oximeter?

Oxyfit Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2022-11-08. The listed applicant is Shenzhen Viatom Technology Co., Ltd.. The 510(k) number is K203812.

When did Oxyfit Pulse Oximeter receive FDA 510(k) clearance?

Oxyfit Pulse Oximeter received FDA 510(k) clearance on 2022-11-08, under 510(k) number K203812.

Who is the listed applicant for Oxyfit Pulse Oximeter?

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

What is the FDA product code for Oxyfit Pulse Oximeter?

The FDA product code for Oxyfit Pulse Oximeter is DQA.

其他以 Shenzhen Viatom Technology 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。

K242876心搏血氧濃度計（PO2、PO2A、PO2B）K193348血壓監測器 K191088檢測美O2血氧濃度計 K190207血壓監測器

相關器械（代碼：DQA）

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。

K252821可重用成人SpO2夾式感測器（3m）（M1196A）；可重用成人SpO2夾式感測器（0.9m）（M1196T）Philips Medizin Systeme Böblingen GmbH K252655心脈血氧濃度計（PO-A2AO、PO-A2AT、PO-A3AO、PO-H1AO、PO-B1AO、PO-C5AO、PO-C5AT、PO-C6AO、PO-C6AT）Shenzhen Imdk Medical Technology Co., Ltd.K253887鼻翼SpO2感測器（989803205381）；鼻翼SpO2感測器（989803205391）；鼻翼Sp02感測器（989803205401）Philips Medizin Systeme K260931Unimed可重用手指夾式SpO2感測器（U403-49R及U103-49R）Unimed Medical Supplies, Inc.K252448AViTA脉搏血氧儀 (SP61)Avita Corporation K252805YUWELL®手指血氧計（YX105、YX106、YX110、YX310）Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。