DEKA SMARTPERIO
K-Number: K213658 · 2022-03-11
ApplicantEl.En Electronic Engineering Spa
Decision Date2022-03-11
Product CodeNVK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
DEKA SMARTPERIO is a medical device manufactured by El.En Electronic Engineering Spa. It received FDA 510(k) clearance on 2022-03-11 under approval number K213658. The device is classified under product code NVK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DEKA SMARTPERIO?
DEKA SMARTPERIO is a medical device that received FDA 510(k) clearance on 2022-03-11. It is manufactured by El.En Electronic Engineering Spa. The 510(k) number is K213658.
When was DEKA SMARTPERIO approved by the FDA?
DEKA SMARTPERIO received FDA 510(k) clearance on 2022-03-11, under approval number K213658.
What company makes DEKA SMARTPERIO?
DEKA SMARTPERIO is manufactured by El.En Electronic Engineering Spa.
What is the FDA product code for DEKA SMARTPERIO?
The FDA product code for DEKA SMARTPERIO is NVK.
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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.