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FDA 510(k)

BAHADIR STERILIZATION TRAYS

K-Number: K102146 · 2010-11-18

Decision Date2010-11-18
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BAHADIR STERILIZATION TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Bahadir USA Corp.. It received FDA 510(k) clearance on 2010-11-18 under 510(k) number K102146. 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 TRAYS?

BAHADIR STERILIZATION TRAYS is a medical device that received FDA 510(k) clearance on 2010-11-18. The listed applicant is Bahadir USA Corp.. The 510(k) number is K102146.

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

BAHADIR STERILIZATION TRAYS received FDA 510(k) clearance on 2010-11-18, under 510(k) number K102146.

Who is the listed applicant for BAHADIR STERILIZATION TRAYS?

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

What is the FDA product code for BAHADIR STERILIZATION TRAYS?

The FDA product code for BAHADIR STERILIZATION TRAYS is KCT.

Related Clinical Trials

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.

Other records listing Bahadir USA Corp. as applicant

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.

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.

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