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FDA 510(k)

CAVIDENTIN

K-Number: K813380 · 1982-02-24

ApplicantBitan Int'L Marketing Co.
Decision Date1982-02-24
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAVIDENTIN is the device name listed in this FDA 510(k) record. The listed applicant is Bitan Int'L Marketing Co.. It received FDA 510(k) clearance on 1982-02-24 under 510(k) number K813380. 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 CAVIDENTIN?

CAVIDENTIN is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Bitan Int'L Marketing Co.. The 510(k) number is K813380.

When did CAVIDENTIN receive FDA 510(k) clearance?

CAVIDENTIN received FDA 510(k) clearance on 1982-02-24, under 510(k) number K813380.

Who is the listed applicant for CAVIDENTIN?

The FDA 510(k) record lists Bitan Int'L Marketing Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAVIDENTIN?

The FDA product code for CAVIDENTIN is EMA.

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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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