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FDA 510(k)

HY-BOND ZINC OXIDE EUGENOL TEMP.

K-Number: K841196 · 1984-05-11

Decision Date1984-05-11
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HY-BOND ZINC OXIDE EUGENOL TEMP. is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corp.. It received FDA 510(k) clearance on 1984-05-11 under 510(k) number K841196. 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 HY-BOND ZINC OXIDE EUGENOL TEMP.?

HY-BOND ZINC OXIDE EUGENOL TEMP. is a medical device that received FDA 510(k) clearance on 1984-05-11. The listed applicant is Shofu Dental Corp.. The 510(k) number is K841196.

When did HY-BOND ZINC OXIDE EUGENOL TEMP. receive FDA 510(k) clearance?

HY-BOND ZINC OXIDE EUGENOL TEMP. received FDA 510(k) clearance on 1984-05-11, under 510(k) number K841196.

Who is the listed applicant for HY-BOND ZINC OXIDE EUGENOL TEMP.?

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

What is the FDA product code for HY-BOND ZINC OXIDE EUGENOL TEMP.?

The FDA product code for HY-BOND ZINC OXIDE EUGENOL TEMP. is EMA.

Related Clinical Trials

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.

Other records listing Shofu Dental Corp. 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.

View all 59 devices →

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.

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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