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FDA 510(k)

SULTAN TOOTH ROOT DESENSITIZER

K-Number: K072342 · 2007-10-03

ApplicantDentsply International, Inc.
Decision Date2007-10-03
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SULTAN TOOTH ROOT DESENSITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply International, Inc.. It received FDA 510(k) clearance on 2007-10-03 under 510(k) number K072342. 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 SULTAN TOOTH ROOT DESENSITIZER?

SULTAN TOOTH ROOT DESENSITIZER is a medical device that received FDA 510(k) clearance on 2007-10-03. The listed applicant is Dentsply International, Inc.. The 510(k) number is K072342.

When did SULTAN TOOTH ROOT DESENSITIZER receive FDA 510(k) clearance?

SULTAN TOOTH ROOT DESENSITIZER received FDA 510(k) clearance on 2007-10-03, under 510(k) number K072342.

Who is the listed applicant for SULTAN TOOTH ROOT DESENSITIZER?

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

What is the FDA product code for SULTAN TOOTH ROOT DESENSITIZER?

The FDA product code for SULTAN TOOTH ROOT DESENSITIZER is LBH.

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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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