FDA 510(k)

RFP-100A 接線 (單次使用)

K 號：K230571 · 2023-05-30

決定日期2023-05-30

產品代碼DSA

諮詢委員會履歷

決定相當於

器材摘要

RFP-100A Connector Cable (Single Use) is the device name listed in this FDA 510(k) record. The listed applicant is Baylis Medical Technologies, Inc.. It received FDA 510(k) clearance on 2023-05-30 under 510(k) number K230571. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the RFP-100A Connector Cable (Single Use)?

RFP-100A Connector Cable (Single Use) is a medical device that received FDA 510(k) clearance on 2023-05-30. The listed applicant is Baylis Medical Technologies, Inc.. The 510(k) number is K230571.

When did RFP-100A Connector Cable (Single Use) receive FDA 510(k) clearance?

RFP-100A Connector Cable (Single Use) received FDA 510(k) clearance on 2023-05-30, under 510(k) number K230571.

Who is the listed applicant for RFP-100A Connector Cable (Single Use)?

The FDA 510(k) record lists Baylis Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RFP-100A Connector Cable (Single Use)?

The FDA product code for RFP-100A Connector Cable (Single Use) is DSA.

其他以 Baylis Medical Technologies, Inc. 為申請人之記錄

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相關器械（代碼：DSA）

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