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FDA 510(k)

LOW FUSING WHITE GOLD

K-Number: K895056 · 1989-12-19

Decision Date1989-12-19
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LOW FUSING WHITE GOLD is the device name listed in this FDA 510(k) record. The listed applicant is Leach and Dillon Co., Inc.. It received FDA 510(k) clearance on 1989-12-19 under 510(k) number K895056. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOW FUSING WHITE GOLD?

LOW FUSING WHITE GOLD is a medical device that received FDA 510(k) clearance on 1989-12-19. The listed applicant is Leach and Dillon Co., Inc.. The 510(k) number is K895056.

When did LOW FUSING WHITE GOLD receive FDA 510(k) clearance?

LOW FUSING WHITE GOLD received FDA 510(k) clearance on 1989-12-19, under 510(k) number K895056.

Who is the listed applicant for LOW FUSING WHITE GOLD?

The FDA 510(k) record lists Leach and Dillon Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOW FUSING WHITE GOLD?

The FDA product code for LOW FUSING WHITE GOLD is EJT.

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 Leach and Dillon Co., Inc. 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 31 devices →

Related Devices (Code: EJT)

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

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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