circul™ pro 環
K 號：K221361 · 2023-08-29
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器材摘要
circul™ pro Ring is the device name listed in this FDA 510(k) record. The listed applicant is Bodimetrics, LLC. It received FDA 510(k) clearance on 2023-08-29 under 510(k) number K221361. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
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.
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相關器械（代碼：DQA）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
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