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FDA 510(k)

STERILIZATION MATS

K-Number: K103226 · 2011-02-18

ApplicantSTERIS Corporation
Decision Date2011-02-18
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILIZATION MATS is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2011-02-18 under 510(k) number K103226. 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 MATS?

STERILIZATION MATS is a medical device that received FDA 510(k) clearance on 2011-02-18. The listed applicant is STERIS Corporation. The 510(k) number is K103226.

When did STERILIZATION MATS receive FDA 510(k) clearance?

STERILIZATION MATS received FDA 510(k) clearance on 2011-02-18, under 510(k) number K103226.

Who is the listed applicant for STERILIZATION MATS?

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

What is the FDA product code for STERILIZATION MATS?

The FDA product code for STERILIZATION MATS is KCT.

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Related Devices (Code: KCT)

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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.

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