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FDA 510(k)

NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN

K-Number: K983966 · 1999-01-29

ApplicantDentsply Intl.
Decision Date1999-01-29
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1999-01-29 under 510(k) number K983966. 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 NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN?

NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN is a medical device that received FDA 510(k) clearance on 1999-01-29. The listed applicant is Dentsply Intl.. The 510(k) number is K983966.

When did NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN receive FDA 510(k) clearance?

NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN received FDA 510(k) clearance on 1999-01-29, under 510(k) number K983966.

Who is the listed applicant for NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN?

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

What is the FDA product code for NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN?

The FDA product code for NUPRO PROPHYLAXIS PASTE WITH FLOURIDE AND TRICLOSAN is EJR.

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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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