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FDA 510(k)

3M CLINPRO PROPHY PASTE, MODEL 12611

K-Number: K990482 · 1999-05-13

ApplicantMinnesota Mining and Mfg. Co.
Decision Date1999-05-13
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

3M CLINPRO PROPHY PASTE, MODEL 12611 is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Mining and Mfg. Co.. It received FDA 510(k) clearance on 1999-05-13 under 510(k) number K990482. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M CLINPRO PROPHY PASTE, MODEL 12611?

3M CLINPRO PROPHY PASTE, MODEL 12611 is a medical device that received FDA 510(k) clearance on 1999-05-13. The listed applicant is Minnesota Mining and Mfg. Co.. The 510(k) number is K990482.

When did 3M CLINPRO PROPHY PASTE, MODEL 12611 receive FDA 510(k) clearance?

3M CLINPRO PROPHY PASTE, MODEL 12611 received FDA 510(k) clearance on 1999-05-13, under 510(k) number K990482.

Who is the listed applicant for 3M CLINPRO PROPHY PASTE, MODEL 12611?

The FDA 510(k) record lists Minnesota Mining and Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M CLINPRO PROPHY PASTE, MODEL 12611?

The FDA product code for 3M CLINPRO PROPHY PASTE, MODEL 12611 is EJR.

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Other records listing Minnesota Mining and Mfg. Co. as applicant

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Related Devices (Code: EJR)

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.

K171189AIR-FLOW PLUS Prophylaxis powderE.M.S Electro Medical Systems S.AK121698NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMINDentsply International, Inc.K103114OSSPRAY SYLC CROsspray, Ltd.K102053BUTLER CALCI-FLOR PROPHYLAXIS PASTESunstar Americas, Inc.K101104REMIN PROVoco GmbHK100539PREVENTECH PROPHYLAXIS PASTE WITH FLUORIDEPreventive Technologies, 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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