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FDA 510(k)

SPARTAN SOLDER

K-Number: K854738 · 1986-03-06

ApplicantWilliams Gold Refining Co., Inc.
Decision Date1986-03-06
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPARTAN SOLDER 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 1986-03-06 under 510(k) number K854738. 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 SPARTAN SOLDER?

SPARTAN SOLDER is a medical device that received FDA 510(k) clearance on 1986-03-06. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K854738.

When did SPARTAN SOLDER receive FDA 510(k) clearance?

SPARTAN SOLDER received FDA 510(k) clearance on 1986-03-06, under 510(k) number K854738.

Who is the listed applicant for SPARTAN SOLDER?

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 SPARTAN SOLDER?

The FDA product code for SPARTAN SOLDER 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 ALLOYSK852895CERAMIC ALLOY NO. DW 179K852093ALLOY 7K850699SPARTAN -ALLOY FOR PORCELAIN FUSED TO METALK844394RENAISSANCE BONDING AGENT

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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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