BAHADIR STERILIZATION CONTAINERS
K-Number: K233578 · 2024-03-22
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.