FDA 510(k)

眼內壓測量儀 EASYTON

K 號：K190382 · 2019-12-06

決定日期2019-12-06

產品代碼HKX

諮詢委員會此為醫療器材法規文本之翻譯。根據醫療法規翻譯政策，以下為繁體中文譯文：本文件概述適用於醫療器材之監管架構，包括美國食品藥物管理局（FDA）之上市前審查程序。第510(k)條途徑適用於與已合法上市器材（predicate device）實質等效之器材，而上市前核准（PMA）則為最高風險等級（Class III）器材所要求。臨床證據可能引用NCT編號之試驗登記，或PMID編號之同行評審文獻。所有產品名稱、公司名稱、識別碼及統一資源定位符（URL）均保留原文，以確保可追溯性及法規提交之完整性。

決定相當於

器材摘要

Intraocular Pressure Tonometer EASYTON is the device name listed in this FDA 510(k) record. The listed applicant is Company Elamed. It received FDA 510(k) clearance on 2019-12-06 under 510(k) number K190382. The device is classified under product code HKX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Intraocular Pressure Tonometer EASYTON?

Intraocular Pressure Tonometer EASYTON is a medical device that received FDA 510(k) clearance on 2019-12-06. The listed applicant is Company Elamed. The 510(k) number is K190382.

When did Intraocular Pressure Tonometer EASYTON receive FDA 510(k) clearance?

Intraocular Pressure Tonometer EASYTON received FDA 510(k) clearance on 2019-12-06, under 510(k) number K190382.

Who is the listed applicant for Intraocular Pressure Tonometer EASYTON?

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

What is the FDA product code for Intraocular Pressure Tonometer EASYTON?

The FDA product code for Intraocular Pressure Tonometer EASYTON is HKX.

相關器械（代碼：HKX）

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。

K253039AUTO KERATO-REFRACTO TONOMETER TRK-3 OMNIATopcon Corporation K223739VS桌面式眼壓計Medimaging Integrated Solution, Inc.K181260MiiS 賀魯斯視野 DPT 100Medimaging Integrated Solution, Inc (Miis)K181143基勒TonoCare眼壓計Keeler Instruments, Inc.K180820Tono Vue 非接觸式眼壓計Crystalvue Medical Corporation K162067VX130 眼科診斷設備Luneau Sas

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。

器材摘要

常見問題

相關臨床試驗

相關器械（代碼：HKX）

官方來源