A-dec 300, A-dec 500
K号: K213932 · 2022-03-02
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申请人A-Dec, Inc.
决定日期2022-03-02
产品代码EIA
咨询委员会DE
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决定实质等同
器械摘要
A-dec 300, A-dec 500 is the device name listed in this FDA 510(k) record. The listed applicant is A-Dec, Inc.. It received FDA 510(k) clearance on 2022-03-02 under 510(k) number K213932. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the A-dec 300, A-dec 500?
A-dec 300, A-dec 500 is a medical device that received FDA 510(k) clearance on 2022-03-02. The listed applicant is A-Dec, Inc.. The 510(k) number is K213932.
When did A-dec 300, A-dec 500 receive FDA 510(k) clearance?
A-dec 300, A-dec 500 received FDA 510(k) clearance on 2022-03-02, under 510(k) number K213932.
Who is the listed applicant for A-dec 300, A-dec 500?
The FDA 510(k) record lists A-Dec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A-dec 300, A-dec 500?
The FDA product code for A-dec 300, A-dec 500 is EIA.
相关器械（代码：EIA）
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