FDA 510(k)

BAHADIR STERILIZATION CONTAINERS

K-Number: K233578 · 2024-03-22

Decision Date2024-03-22

Product CodeKCT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BAHADIR STERILIZATION CONTAINERS is a medical device manufactured by Bahadir USA, LLC. It received FDA 510(k) clearance on 2024-03-22 under approval number K233578. 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 BAHADIR STERILIZATION CONTAINERS?

BAHADIR STERILIZATION CONTAINERS is a medical device that received FDA 510(k) clearance on 2024-03-22. It is manufactured by Bahadir USA, LLC. The 510(k) number is K233578.

When was BAHADIR STERILIZATION CONTAINERS approved by the FDA?

BAHADIR STERILIZATION CONTAINERS received FDA 510(k) clearance on 2024-03-22, under approval number K233578.

What company makes BAHADIR STERILIZATION CONTAINERS?

BAHADIR STERILIZATION CONTAINERS is manufactured by Bahadir USA, LLC.

What is the FDA product code for BAHADIR STERILIZATION CONTAINERS?

The FDA product code for BAHADIR STERILIZATION CONTAINERS is KCT.

Related Devices (Code: KCT)

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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.