Tablet Application
K-Number: K203566 · 2021-05-13
ApplicantSmith & Nephew
Decision Date2021-05-13
Product CodeODA
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Tablet Application is a medical device manufactured by Smith & Nephew. It received FDA 510(k) clearance on 2021-05-13 under approval number K203566. The device is classified under product code ODA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Tablet Application?
Tablet Application is a medical device that received FDA 510(k) clearance on 2021-05-13. It is manufactured by Smith & Nephew. The 510(k) number is K203566.
When was Tablet Application approved by the FDA?
Tablet Application received FDA 510(k) clearance on 2021-05-13, under approval number K203566.
What company makes Tablet Application?
Tablet Application is manufactured by Smith & Nephew.
What is the FDA product code for Tablet Application?
The FDA product code for Tablet Application is ODA.
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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.