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FDA 510(k)

SILCOT COPAL CAVITY VARNISH

K-Number: K895798 · 1989-12-21

ApplicantSpecialites Septodont
Decision Date1989-12-21
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SILCOT COPAL CAVITY VARNISH is the device name listed in this FDA 510(k) record. The listed applicant is Specialites Septodont. It received FDA 510(k) clearance on 1989-12-21 under 510(k) number K895798. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILCOT COPAL CAVITY VARNISH?

SILCOT COPAL CAVITY VARNISH is a medical device that received FDA 510(k) clearance on 1989-12-21. The listed applicant is Specialites Septodont. The 510(k) number is K895798.

When did SILCOT COPAL CAVITY VARNISH receive FDA 510(k) clearance?

SILCOT COPAL CAVITY VARNISH received FDA 510(k) clearance on 1989-12-21, under 510(k) number K895798.

Who is the listed applicant for SILCOT COPAL CAVITY VARNISH?

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

What is the FDA product code for SILCOT COPAL CAVITY VARNISH?

The FDA product code for SILCOT COPAL CAVITY VARNISH is EMA.

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Other records listing Specialites Septodont as applicant

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.

K012427PHARMAETHYL LOCAL PULP AND VITALITY TESTING AGENTK010415ISODANK982773QUICKSET LIQUID AND POWDERK982671SECURALLOYK980633ENDOSOLV EK920692SEPTOCALCINE ULTRA

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Related Devices (Code: EMA)

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.

K262983EsTemp ImplantSpident Co., Ltd.K254201Any-CemMediclus Co., Ltd.K261937PacTemp Automix NEThe Belport Company Inc., DBA Gingi-PakK261166DIA-CEMDiaDent Group InternationalK254109G-CEM UNIVERSALGC America, Inc.K253337REGEN Bioactive CementInter-Med, 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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