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FDA 510(k)

Sterilization Tray

K-Number: K160912 · 2016-10-07

Decision Date2016-10-07
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sterilization Tray is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2016-10-07 under approval number K160912. 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 Sterilization Tray?

Sterilization Tray is a medical device that received FDA 510(k) clearance on 2016-10-07. It is manufactured by STERIS Corporation. The 510(k) number is K160912.

When was Sterilization Tray approved by the FDA?

Sterilization Tray received FDA 510(k) clearance on 2016-10-07, under approval number K160912.

What company makes Sterilization Tray?

Sterilization Tray is manufactured by STERIS Corporation.

What is the FDA product code for Sterilization Tray?

The FDA product code for Sterilization Tray is KCT.

Other Devices by STERIS Corporation

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Related Devices (Code: KCT)

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.