Anatase Navi Disposable Instrument
K-Number: K241625 · 2024-07-05
ApplicantRemex Medical Corp.
Decision Date2024-07-05
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Anatase Navi Disposable Instrument is a medical device manufactured by Remex Medical Corp.. It received FDA 510(k) clearance on 2024-07-05 under approval number K241625. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Anatase Navi Disposable Instrument?
Anatase Navi Disposable Instrument is a medical device that received FDA 510(k) clearance on 2024-07-05. It is manufactured by Remex Medical Corp.. The 510(k) number is K241625.
When was Anatase Navi Disposable Instrument approved by the FDA?
Anatase Navi Disposable Instrument received FDA 510(k) clearance on 2024-07-05, under approval number K241625.
What company makes Anatase Navi Disposable Instrument?
Anatase Navi Disposable Instrument is manufactured by Remex Medical Corp..
What is the FDA product code for Anatase Navi Disposable Instrument?
The FDA product code for Anatase Navi Disposable Instrument is OLO.
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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.