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FDA 510(k)

DENTIN DESENSITIZER AGENT

K-Number: K073117 · 2007-12-19

ApplicantDentsply Intl., Inc.
Decision Date2007-12-19
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTIN DESENSITIZER AGENT is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl., Inc.. It received FDA 510(k) clearance on 2007-12-19 under 510(k) number K073117. 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 DENTIN DESENSITIZER AGENT?

DENTIN DESENSITIZER AGENT is a medical device that received FDA 510(k) clearance on 2007-12-19. The listed applicant is Dentsply Intl., Inc.. The 510(k) number is K073117.

When did DENTIN DESENSITIZER AGENT receive FDA 510(k) clearance?

DENTIN DESENSITIZER AGENT received FDA 510(k) clearance on 2007-12-19, under 510(k) number K073117.

Who is the listed applicant for DENTIN DESENSITIZER AGENT?

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

What is the FDA product code for DENTIN DESENSITIZER AGENT?

The FDA product code for DENTIN DESENSITIZER AGENT 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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