Silhouette Featherlift / Silhouette Lift
K-Number: K191299 · 2019-06-14
ApplicantSilhouette Lift, Inc.
Decision Date2019-06-14
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Silhouette Featherlift / Silhouette Lift is a medical device manufactured by Silhouette Lift, Inc.. It received FDA 510(k) clearance on 2019-06-14 under approval number K191299. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Silhouette Featherlift / Silhouette Lift?
Silhouette Featherlift / Silhouette Lift is a medical device that received FDA 510(k) clearance on 2019-06-14. It is manufactured by Silhouette Lift, Inc.. The 510(k) number is K191299.
When was Silhouette Featherlift / Silhouette Lift approved by the FDA?
Silhouette Featherlift / Silhouette Lift received FDA 510(k) clearance on 2019-06-14, under approval number K191299.
What company makes Silhouette Featherlift / Silhouette Lift?
Silhouette Featherlift / Silhouette Lift is manufactured by Silhouette Lift, Inc..
What is the FDA product code for Silhouette Featherlift / Silhouette Lift?
The FDA product code for Silhouette Featherlift / Silhouette Lift is GAW.
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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.