Anthogyr Surgical Cassettes
K-Number: K230680 · 2023-07-11
ApplicantAnthogyr
Decision Date2023-07-11
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Anthogyr Surgical Cassettes is a medical device manufactured by Anthogyr. It received FDA 510(k) clearance on 2023-07-11 under approval number K230680. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Anthogyr Surgical Cassettes?
Anthogyr Surgical Cassettes is a medical device that received FDA 510(k) clearance on 2023-07-11. It is manufactured by Anthogyr. The 510(k) number is K230680.
When was Anthogyr Surgical Cassettes approved by the FDA?
Anthogyr Surgical Cassettes received FDA 510(k) clearance on 2023-07-11, under approval number K230680.
What company makes Anthogyr Surgical Cassettes?
Anthogyr Surgical Cassettes is manufactured by Anthogyr.
What is the FDA product code for Anthogyr Surgical Cassettes?
The FDA product code for Anthogyr Surgical Cassettes is KCT.
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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.