FDA 510(k)

BNLE亲水涂层外周导丝

K号: K232662 · 2024-05-14

决定日期2024-05-14

产品代码DQX

咨询委员会CV 请注意，由于原文未提供具体内容，以下是一个示例翻译： --- 产品名称：[产品名称] 公司名称：[公司名称] FDA批准号：[FDA批准号] 510(k)申请号：[510(k)申请号] PMA申请号：[PMA申请号] 临床试验注册号：[NCT] PubMed ID：[PMID] 产品标识符：[标识符] 产品URL：[URL] --- 请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。

决定实质等同

器械摘要

BNLE Hydrophilic Jacketed Peripheral Guidewire is the device name listed in this FDA 510(k) record. The listed applicant is Biomerics Nle. It received FDA 510(k) clearance on 2024-05-14 under 510(k) number K232662. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BNLE Hydrophilic Jacketed Peripheral Guidewire?

BNLE Hydrophilic Jacketed Peripheral Guidewire is a medical device that received FDA 510(k) clearance on 2024-05-14. The listed applicant is Biomerics Nle. The 510(k) number is K232662.

When did BNLE Hydrophilic Jacketed Peripheral Guidewire receive FDA 510(k) clearance?

BNLE Hydrophilic Jacketed Peripheral Guidewire received FDA 510(k) clearance on 2024-05-14, under 510(k) number K232662.

Who is the listed applicant for BNLE Hydrophilic Jacketed Peripheral Guidewire?

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

What is the FDA product code for BNLE Hydrophilic Jacketed Peripheral Guidewire?

The FDA product code for BNLE Hydrophilic Jacketed Peripheral Guidewire is DQX.

列明Biomerics Nle为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K221390BNLE通路导丝

官方来源

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