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FDA 510(k)

ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT

K-Number: K082071 · 2008-10-02

ApplicantAdpharma, Inc.
Decision Date2008-10-02
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT is the device name listed in this FDA 510(k) record. The listed applicant is Adpharma, Inc.. It received FDA 510(k) clearance on 2008-10-02 under 510(k) number K082071. 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 ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT?

ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT is a medical device that received FDA 510(k) clearance on 2008-10-02. The listed applicant is Adpharma, Inc.. The 510(k) number is K082071.

When did ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT receive FDA 510(k) clearance?

ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT received FDA 510(k) clearance on 2008-10-02, under 510(k) number K082071.

Who is the listed applicant for ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT?

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

What is the FDA product code for ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT?

The FDA product code for ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT is LBH.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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