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FDA 510(k)

TransForm McCarthy Mitral Annuloplasty Ring (TF)

K-Number: K232599 · 2024-04-09

Decision Date2024-04-09
Product CodeKRH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TransForm McCarthy Mitral Annuloplasty Ring (TF) is a medical device manufactured by Genesee Biomedical, Inc.. It received FDA 510(k) clearance on 2024-04-09 under approval number K232599. The device is classified under product code KRH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TransForm McCarthy Mitral Annuloplasty Ring (TF)?

TransForm McCarthy Mitral Annuloplasty Ring (TF) is a medical device that received FDA 510(k) clearance on 2024-04-09. It is manufactured by Genesee Biomedical, Inc.. The 510(k) number is K232599.

When was TransForm McCarthy Mitral Annuloplasty Ring (TF) approved by the FDA?

TransForm McCarthy Mitral Annuloplasty Ring (TF) received FDA 510(k) clearance on 2024-04-09, under approval number K232599.

What company makes TransForm McCarthy Mitral Annuloplasty Ring (TF)?

TransForm McCarthy Mitral Annuloplasty Ring (TF) is manufactured by Genesee Biomedical, Inc..

What is the FDA product code for TransForm McCarthy Mitral Annuloplasty Ring (TF)?

The FDA product code for TransForm McCarthy Mitral Annuloplasty Ring (TF) is KRH.

Related Clinical Trials

Other Devices by Genesee Biomedical, Inc.

Related Devices (Code: KRH)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.