LC GLOSSFILL XR
K-Number: K182778 · 2019-04-22
Decision Date2019-04-22
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
LC GLOSSFILL XR is a medical device manufactured by S&C Polymer Silicon- Und Composite Spezialitaeten GmbH. It received FDA 510(k) clearance on 2019-04-22 under approval number K182778. 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 GLOSSFILL XR?
LC GLOSSFILL XR is a medical device that received FDA 510(k) clearance on 2019-04-22. It is manufactured by S&C Polymer Silicon- Und Composite Spezialitaeten GmbH. The 510(k) number is K182778.
When was LC GLOSSFILL XR approved by the FDA?
LC GLOSSFILL XR received FDA 510(k) clearance on 2019-04-22, under approval number K182778.
What company makes LC GLOSSFILL XR?
LC GLOSSFILL XR is manufactured by S&C Polymer Silicon- Und Composite Spezialitaeten GmbH.
What is the FDA product code for LC GLOSSFILL XR?
The FDA product code for LC GLOSSFILL XR 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.