Stylus
K-Number: K233591 · 2024-05-31
ApplicantDegania Silicone , Ltd.
Decision Date2024-05-31
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Stylus is a medical device manufactured by Degania Silicone , Ltd.. It received FDA 510(k) clearance on 2024-05-31 under approval number K233591. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Stylus?
Stylus is a medical device that received FDA 510(k) clearance on 2024-05-31. It is manufactured by Degania Silicone , Ltd.. The 510(k) number is K233591.
When was Stylus approved by the FDA?
Stylus received FDA 510(k) clearance on 2024-05-31, under approval number K233591.
What company makes Stylus?
Stylus is manufactured by Degania Silicone , Ltd..
What is the FDA product code for Stylus?
The FDA product code for Stylus is KNT.
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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.