Silhouette InstaLift
K-Number: K163676 · 2017-06-16
ApplicantSilhouette Lift, Inc.
Decision Date2017-06-16
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Silhouette InstaLift is a medical device manufactured by Silhouette Lift, Inc.. It received FDA 510(k) clearance on 2017-06-16 under approval number K163676. The device is classified under product code GAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Silhouette InstaLift?
Silhouette InstaLift is a medical device that received FDA 510(k) clearance on 2017-06-16. It is manufactured by Silhouette Lift, Inc.. The 510(k) number is K163676.
When was Silhouette InstaLift approved by the FDA?
Silhouette InstaLift received FDA 510(k) clearance on 2017-06-16, under approval number K163676.
What company makes Silhouette InstaLift?
Silhouette InstaLift is manufactured by Silhouette Lift, Inc..
What is the FDA product code for Silhouette InstaLift?
The FDA product code for Silhouette InstaLift is GAM.
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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.