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FDA 510(k)

DISC, WILL-CERUM LIQUID

K-Number: K760514 · 1976-09-03

ApplicantWilliams Gold Refining Co., Inc.
Decision Date1976-09-03
Product Code
DecisionSubstantially Equivalent

Device Summary

DISC, WILL-CERUM LIQUID 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 1976-09-03 under 510(k) number K760514. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISC, WILL-CERUM LIQUID?

DISC, WILL-CERUM LIQUID is a medical device that received FDA 510(k) clearance on 1976-09-03. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K760514.

When did DISC, WILL-CERUM LIQUID receive FDA 510(k) clearance?

DISC, WILL-CERUM LIQUID received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760514.

Who is the listed applicant for DISC, WILL-CERUM LIQUID?

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

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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 SOLDERK852895CERAMIC ALLOY NO. DW 179K852093ALLOY 7K850699SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL

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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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