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FDA 510(k)

DENTANURSE

K-Number: K891607 · 1989-08-11

ApplicantThe Irish Scene
Decision Date1989-08-11
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTANURSE is the device name listed in this FDA 510(k) record. The listed applicant is The Irish Scene. It received FDA 510(k) clearance on 1989-08-11 under 510(k) number K891607. 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 DENTANURSE?

DENTANURSE is a medical device that received FDA 510(k) clearance on 1989-08-11. The listed applicant is The Irish Scene. The 510(k) number is K891607.

When did DENTANURSE receive FDA 510(k) clearance?

DENTANURSE received FDA 510(k) clearance on 1989-08-11, under 510(k) number K891607.

Who is the listed applicant for DENTANURSE?

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

What is the FDA product code for DENTANURSE?

The FDA product code for DENTANURSE 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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