circul pro Ring
K-Number: K221361 · 2023-08-29
ApplicantBodimetrics, LLC
Decision Date2023-08-29
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
circul pro Ring is a medical device manufactured by Bodimetrics, LLC. It received FDA 510(k) clearance on 2023-08-29 under approval number K221361. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the circul pro Ring?
circul pro Ring is a medical device that received FDA 510(k) clearance on 2023-08-29. It is manufactured by Bodimetrics, LLC. The 510(k) number is K221361.
When was circul pro Ring approved by the FDA?
circul pro Ring received FDA 510(k) clearance on 2023-08-29, under approval number K221361.
What company makes circul pro Ring?
circul pro Ring is manufactured by Bodimetrics, LLC.
What is the FDA product code for circul pro Ring?
The FDA product code for circul pro Ring is DQA.
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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.