circul™ pro Ring
K-Number: K221361 · 2023-08-29
Device Summary
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. The listed applicant is Bodimetrics, LLC. The 510(k) number is K221361.
When did circul™ pro Ring receive FDA 510(k) clearance?
circul™ pro Ring received FDA 510(k) clearance on 2023-08-29, under 510(k) number K221361.
Who is the listed applicant for circul™ pro Ring?
The FDA 510(k) record lists Bodimetrics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for circul™ pro Ring?
The FDA product code for circul™ pro Ring is DQA.
Related Devices (Code: DQA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.