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FDA 510(k)

ACCU-STAIN

K-Number: K771887 · 1977-11-14

ApplicantWilliams Gold Refining Co., Inc.
Decision Date1977-11-14
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACCU-STAIN 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 1977-11-14 under 510(k) number K771887. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU-STAIN?

ACCU-STAIN is a medical device that received FDA 510(k) clearance on 1977-11-14. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K771887.

When did ACCU-STAIN receive FDA 510(k) clearance?

ACCU-STAIN received FDA 510(k) clearance on 1977-11-14, under 510(k) number K771887.

Who is the listed applicant for ACCU-STAIN?

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 ACCU-STAIN?

The FDA product code for ACCU-STAIN is EIH.

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

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Related Devices (Code: EIH)

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.

K262074Any-ZircosMediclus Co., Ltd.K262239Obsidian® Press Over ZirconiaPrismatik Dentalcraft, Inc.K261046Dental Zirconia Blank & Coloring LiquidHunan Qinghao Puzhong Technology Co., Ltd.K262195Dandy Ceramic Stain and GlazeZima International Inc., dba DandyK260918Zolid LunarisAmann Girrbach AGK260859Rosetta SM, Rosetta SPHass Corp.

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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