FDA 510(k)

TRACOE vario

K号: K203362 · 2021-08-05

决定日期2021-08-05

产品代码JOH

咨询委员会AN 请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。

决定实质等同

器械摘要

TRACOE vario is the device name listed in this FDA 510(k) record. The listed applicant is Tracoe Medical GmbH. It received FDA 510(k) clearance on 2021-08-05 under 510(k) number K203362. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the TRACOE vario?

TRACOE vario is a medical device that received FDA 510(k) clearance on 2021-08-05. The listed applicant is Tracoe Medical GmbH. The 510(k) number is K203362.

When did TRACOE vario receive FDA 510(k) clearance?

TRACOE vario received FDA 510(k) clearance on 2021-08-05, under 510(k) number K203362.

Who is the listed applicant for TRACOE vario?

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

What is the FDA product code for TRACOE vario?

The FDA product code for TRACOE vario is JOH.

列明Tracoe Medical GmbH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。

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相关器械（代码：JOH）

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。

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官方来源

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