LC ChromeFlow
K-Number: K222445 · 2023-03-06
Decision Date2023-03-06
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
LC ChromeFlow is a medical device manufactured by S&C Polymer Silicon- Und Composite Spezialitaten GmbH. It received FDA 510(k) clearance on 2023-03-06 under approval number K222445. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LC ChromeFlow?
LC ChromeFlow is a medical device that received FDA 510(k) clearance on 2023-03-06. It is manufactured by S&C Polymer Silicon- Und Composite Spezialitaten GmbH. The 510(k) number is K222445.
When was LC ChromeFlow approved by the FDA?
LC ChromeFlow received FDA 510(k) clearance on 2023-03-06, under approval number K222445.
What company makes LC ChromeFlow?
LC ChromeFlow is manufactured by S&C Polymer Silicon- Und Composite Spezialitaten GmbH.
What is the FDA product code for LC ChromeFlow?
The FDA product code for LC ChromeFlow is EBF.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.