FDA 510(k)

CEREGLIDE 42中间导管；CEREGLIDE 57中间导管

K号: K241244 · 2024-10-16

决定日期2024-10-16

产品代码QJP

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决定实质等同

器械摘要

CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Cerenovus, Inc.. It received FDA 510(k) clearance on 2024-10-16 under 510(k) number K241244. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter?

CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter is a medical device that received FDA 510(k) clearance on 2024-10-16. The listed applicant is Cerenovus, Inc.. The 510(k) number is K241244.

When did CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter receive FDA 510(k) clearance?

CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter received FDA 510(k) clearance on 2024-10-16, under 510(k) number K241244.

Who is the listed applicant for CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter?

FDA 510(k)记录中列出Cerenovus, Inc.为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter?

The FDA product code for CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter is QJP.

列明Cerenovus, Inc.为申报人的其他记录

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