FDA 510(k)

STERILOX LIQUID CHEMICAL STERILANT SYSTEM

K-Number: K013280 · 2002-09-18

Decision Date2002-09-18

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STERILOX LIQUID CHEMICAL STERILANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sterilox Technologies, Inc.. It received FDA 510(k) clearance on 2002-09-18 under 510(k) number K013280. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILOX LIQUID CHEMICAL STERILANT SYSTEM?

STERILOX LIQUID CHEMICAL STERILANT SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-18. The listed applicant is Sterilox Technologies, Inc.. The 510(k) number is K013280.

When did STERILOX LIQUID CHEMICAL STERILANT SYSTEM receive FDA 510(k) clearance?

STERILOX LIQUID CHEMICAL STERILANT SYSTEM received FDA 510(k) clearance on 2002-09-18, under 510(k) number K013280.

Who is the listed applicant for STERILOX LIQUID CHEMICAL STERILANT SYSTEM?

The FDA 510(k) record lists Sterilox Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILOX LIQUID CHEMICAL STERILANT SYSTEM?

The FDA product code for STERILOX LIQUID CHEMICAL STERILANT SYSTEM is MED.

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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.