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FDA 510(k)

AIROCIDE TI02

K-Number: K023830 · 2003-02-04

ApplicantKes Science & Technology, Inc.
Decision Date2003-02-04
Product CodeFRA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AIROCIDE TI02 is the device name listed in this FDA 510(k) record. The listed applicant is Kes Science & Technology, Inc.. It received FDA 510(k) clearance on 2003-02-04 under 510(k) number K023830. The device is classified under product code FRA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIROCIDE TI02?

AIROCIDE TI02 is a medical device that received FDA 510(k) clearance on 2003-02-04. The listed applicant is Kes Science & Technology, Inc.. The 510(k) number is K023830.

When did AIROCIDE TI02 receive FDA 510(k) clearance?

AIROCIDE TI02 received FDA 510(k) clearance on 2003-02-04, under 510(k) number K023830.

Who is the listed applicant for AIROCIDE TI02?

The FDA 510(k) record lists Kes Science & Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIROCIDE TI02?

The FDA product code for AIROCIDE TI02 is FRA.

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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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