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FDA 510(k)

POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL

K-Number: K895988 · 1990-03-07

ApplicantMilton Hodosh, M.D.
Decision Date1990-03-07
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL is the device name listed in this FDA 510(k) record. The listed applicant is Milton Hodosh, M.D.. It received FDA 510(k) clearance on 1990-03-07 under 510(k) number K895988. 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 POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL?

POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL is a medical device that received FDA 510(k) clearance on 1990-03-07. The listed applicant is Milton Hodosh, M.D.. The 510(k) number is K895988.

When did POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL receive FDA 510(k) clearance?

POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL received FDA 510(k) clearance on 1990-03-07, under 510(k) number K895988.

Who is the listed applicant for POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL?

The FDA 510(k) record lists Milton Hodosh, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL?

The FDA product code for POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL is EMA.

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Other records listing Milton Hodosh, M.D. 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.

K032175DESENS-IONOMERK031721COMPOSITE RESTORATION MATERIALK022025MODIFICATION TO POTASSIUM NITRATE-POLYCARBOXYLATE DENTAL CEMENTK925207GLASS IONOMER CEMENTK905582POTASSIUM NITRATE COMPOSITE RESTORATION PIT ANDK882417POTASSIUM NITRATE POLYCARBOXYLATE DENTAL CEMENT

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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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