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FDA 510(k)

CHLORAPREP

K-Number: K021131 · 2002-09-26

ApplicantCentrix, Inc.
Decision Date2002-09-26
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CHLORAPREP is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 2002-09-26 under 510(k) number K021131. 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 CHLORAPREP?

CHLORAPREP is a medical device that received FDA 510(k) clearance on 2002-09-26. The listed applicant is Centrix, Inc.. The 510(k) number is K021131.

When did CHLORAPREP receive FDA 510(k) clearance?

CHLORAPREP received FDA 510(k) clearance on 2002-09-26, under 510(k) number K021131.

Who is the listed applicant for CHLORAPREP?

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

What is the FDA product code for CHLORAPREP?

The FDA product code for CHLORAPREP is LBH.

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Other records listing Centrix, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250714FluoroDose VarnishK222459Centrix FluoroSilver Silver Diamine Fluoride 38%K152826NoCordK120176SENZZZZZ AWAYK111348RE / STASIS (TM) GINGIVAL RETRACTION PASTEK092384LIQUICORD

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Related Devices (Code: LBH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262243Profisil FreeKettenbach GmbH & Co. KGK253052Fluoride Varnish (Type A,Type C)Nagy Oral Technology Qinhuangdao Co., Ltd.K252073VOCO Profluorid Varnish + BioMinVoco GmbHK261404UltraEZUltradent Products, Inc.K260830APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)Sangi Co., Ltd.K250714FluoroDose VarnishCentrix, Inc.

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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