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FDA 510(k)

CLINPRO PROPHY POWDER

K-Number: K021450 · 2002-08-01

Applicant3M Espe AG Dental Products
Decision Date2002-08-01
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLINPRO PROPHY POWDER is the device name listed in this FDA 510(k) record. The listed applicant is 3M Espe AG Dental Products. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K021450. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINPRO PROPHY POWDER?

CLINPRO PROPHY POWDER is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is 3M Espe AG Dental Products. The 510(k) number is K021450.

When did CLINPRO PROPHY POWDER receive FDA 510(k) clearance?

CLINPRO PROPHY POWDER received FDA 510(k) clearance on 2002-08-01, under 510(k) number K021450.

Who is the listed applicant for CLINPRO PROPHY POWDER?

The FDA 510(k) record lists 3M Espe AG Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLINPRO PROPHY POWDER?

The FDA product code for CLINPRO PROPHY POWDER is KOJ.

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Other records listing 3M Espe AG Dental Products 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.

K100908UNICEM HMK100756MALTAK094007UNICEMK093721COSP2K091826ELEGANTK090718BELLUS SHADING KIT

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Related Devices (Code: KOJ)

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.

K251425turbodent touchMectron S.P.A.K063236BETA-POWDERBrainbase CorporationK042872RONDOFLEX PLUS 360Kavo America CorporationK033675PROSMILE AIR POLISHER AND PROPHYLAXIS POWDERSirona Dental Systems GmbHK033215PREPAIRDanville Materials, Inc.K024105VELOPEX AQUACUT FLUID ABRASION UNITVelopex International, 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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