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FDA 510(k)

DURA-VAC

K-Number: K770545 · 1977-03-24

ApplicantWilliams Gold Refining Co., Inc.
Decision Date1977-03-24
Product Code
DecisionSubstantially Equivalent

Device Summary

DURA-VAC 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 1977-03-24 under 510(k) number K770545. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DURA-VAC?

DURA-VAC is a medical device that received FDA 510(k) clearance on 1977-03-24. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K770545.

When did DURA-VAC receive FDA 510(k) clearance?

DURA-VAC received FDA 510(k) clearance on 1977-03-24, under 510(k) number K770545.

Who is the listed applicant for DURA-VAC?

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

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

View all 26 devices →

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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