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FDA 510(k)

CERAMIC ALLOY NO. DW 179

K-Number: K852895 · 1985-10-21

ApplicantWilliams Gold Refining Co., Inc.
Decision Date1985-10-21
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERAMIC ALLOY NO. DW 179 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 1985-10-21 under 510(k) number K852895. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERAMIC ALLOY NO. DW 179?

CERAMIC ALLOY NO. DW 179 is a medical device that received FDA 510(k) clearance on 1985-10-21. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K852895.

When did CERAMIC ALLOY NO. DW 179 receive FDA 510(k) clearance?

CERAMIC ALLOY NO. DW 179 received FDA 510(k) clearance on 1985-10-21, under 510(k) number K852895.

Who is the listed applicant for CERAMIC ALLOY NO. DW 179?

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 CERAMIC ALLOY NO. DW 179?

The FDA product code for CERAMIC ALLOY NO. DW 179 is EJH.

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Other records listing Williams Gold Refining 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.

K855182ALLOY FOR METAL CROWN & BRIDGE YELLOW PD #46 & #65K860439DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYSK854738SPARTAN SOLDERK852093ALLOY 7K850699SPARTAN -ALLOY FOR PORCELAIN FUSED TO METALK844395RENAISSANCE

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Related Devices (Code: EJH)

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.

K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & COK040180CONTINUM VAalba Dent, Inc.K040179CONTINUMAalba Dent, Inc.K033356VERASOFT ESAalba Dent, Inc.K033045DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECASTAmerican Green Dent. Mfg, Inc.K032136WIROBOND CBego U.S.A.

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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