FDA 510(k)

貝利斯連接線

K 號：K254114 · 2026-01-18

決定日期2026-01-18

產品代碼DSA

諮詢委員會履歷

決定相當於

器材摘要

Baylis Connector Cable 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 2026-01-18 under 510(k) number K254114. 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 Baylis Connector Cable?

Baylis Connector Cable is a medical device that received FDA 510(k) clearance on 2026-01-18. The listed applicant is Baylis Medical Technologies, Inc.. The 510(k) number is K254114.

When did Baylis Connector Cable receive FDA 510(k) clearance?

Baylis Connector Cable received FDA 510(k) clearance on 2026-01-18, under 510(k) number K254114.

Who is the listed applicant for Baylis Connector Cable?

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 Baylis Connector Cable?

The FDA product code for Baylis Connector Cable is DSA.

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

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K250275精確步驟™ 體外放射頻穿刺發生器及精確步驟™ 腳踏開關 K251158PowerWire® 14 電波導絲套件 K232562PowerWire 電波頻率導絲套件 K230571RFP-100A 接線 (單次使用)

相關器械（代碼：DSA）

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官方來源

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