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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 the device name listed in this FDA 510(k) record. The listed applicant is Bahadir USA, LLC. It received FDA 510(k) clearance on 2024-03-22 under 510(k) 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. The listed applicant is Bahadir USA, LLC. The 510(k) number is K233578.

When did BAHADIR STERILIZATION CONTAINERS receive FDA 510(k) clearance?

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

Who is the listed applicant for BAHADIR STERILIZATION CONTAINERS?

The FDA 510(k) record lists Bahadir USA, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAHADIR STERILIZATION CONTAINERS?

The FDA product code for BAHADIR STERILIZATION CONTAINERS is KCT.

Related Devices (Code: KCT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.