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FDA 510(k)

PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS

K-Number: K811563 · 1981-07-28

ApplicantWilliams Gold Refining Co., Inc.
Decision Date1981-07-28
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS is the device name listed in this FDA 510(k) record. The listed applicant is Williams Gold Refining Co., Inc.. It received FDA 510(k) clearance on 1981-07-28 under 510(k) number K811563. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS?

PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K811563.

When did PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS receive FDA 510(k) clearance?

PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811563.

Who is the listed applicant for PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS?

The FDA 510(k) record lists Williams Gold Refining Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS?

The FDA product code for PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS is EJS.

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Other records listing Williams Gold Refining Co., Inc. as applicant

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Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

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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