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FDA 510(k)

AQUEOUS ACRYLIC DISPERSION 28% W/W

K-Number: K023671 · 2002-11-25

ApplicantChx Technologies, Inc.
Decision Date2002-11-25
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AQUEOUS ACRYLIC DISPERSION 28% W/W is the device name listed in this FDA 510(k) record. The listed applicant is Chx Technologies, Inc.. It received FDA 510(k) clearance on 2002-11-25 under 510(k) number K023671. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUEOUS ACRYLIC DISPERSION 28% W/W?

AQUEOUS ACRYLIC DISPERSION 28% W/W is a medical device that received FDA 510(k) clearance on 2002-11-25. The listed applicant is Chx Technologies, Inc.. The 510(k) number is K023671.

When did AQUEOUS ACRYLIC DISPERSION 28% W/W receive FDA 510(k) clearance?

AQUEOUS ACRYLIC DISPERSION 28% W/W received FDA 510(k) clearance on 2002-11-25, under 510(k) number K023671.

Who is the listed applicant for AQUEOUS ACRYLIC DISPERSION 28% W/W?

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

What is the FDA product code for AQUEOUS ACRYLIC DISPERSION 28% W/W?

The FDA product code for AQUEOUS ACRYLIC DISPERSION 28% W/W is LBH.

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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.

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