FDA 510(k)

LC ChromeFlow

K号: K222445 · 2023-03-06

申请人S&C Polymer Silicon- Und Composite Spezialitaten GmbH

决定日期2023-03-06

产品代码EBF

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决定实质等同

器械摘要

LC ChromeFlow is the device name listed in this FDA 510(k) record. The listed applicant is S&C Polymer Silicon- Und Composite Spezialitaten GmbH. It received FDA 510(k) clearance on 2023-03-06 under 510(k) number K222445. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LC ChromeFlow?

LC ChromeFlow is a medical device that received FDA 510(k) clearance on 2023-03-06. The listed applicant is S&C Polymer Silicon- Und Composite Spezialitaten GmbH. The 510(k) number is K222445.

When did LC ChromeFlow receive FDA 510(k) clearance?

LC ChromeFlow received FDA 510(k) clearance on 2023-03-06, under 510(k) number K222445.

Who is the listed applicant for LC ChromeFlow?

The FDA 510(k) record lists S&C Polymer Silicon- Und Composite Spezialitaten GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LC ChromeFlow?

The FDA product code for LC ChromeFlow is EBF.

列明S&C Polymer Silicon- Und Composite Spezialitaten GmbH为申报人的其他记录

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