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FDA 510(k)

ARGEBOND 77+

K-Number: K915165 · 1992-04-21

ApplicantArgen Precious Metals, Inc.
Decision Date1992-04-21
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ARGEBOND 77+ is the device name listed in this FDA 510(k) record. The listed applicant is Argen Precious Metals, Inc.. It received FDA 510(k) clearance on 1992-04-21 under 510(k) number K915165. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGEBOND 77+?

ARGEBOND 77+ is a medical device that received FDA 510(k) clearance on 1992-04-21. The listed applicant is Argen Precious Metals, Inc.. The 510(k) number is K915165.

When did ARGEBOND 77+ receive FDA 510(k) clearance?

ARGEBOND 77+ received FDA 510(k) clearance on 1992-04-21, under 510(k) number K915165.

Who is the listed applicant for ARGEBOND 77+?

The FDA 510(k) record lists Argen Precious Metals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARGEBOND 77+?

The FDA product code for ARGEBOND 77+ is EJS.

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Other records listing Argen Precious Metals, 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.

K965216ARGI-SATIN OR OPTI0-STARK961352285 SLK961211ARGELITE 52+K961285ARGEDENT 40(GOLD-PALLADIUM-SILVER ALLOY FOR PORCELAIN APPLICATION)K954362ARGISTAR 74K954360ARGESOL 600

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Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

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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