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FDA 510(k)

ARGILITE 3

K-Number: K904467 · 1990-10-31

ApplicantArgen Precious Metals, Inc.
Decision Date1990-10-31
Product CodeEIT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ARGILITE 3 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 1990-10-31 under 510(k) number K904467. The device is classified under product code EIT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGILITE 3?

ARGILITE 3 is a medical device that received FDA 510(k) clearance on 1990-10-31. The listed applicant is Argen Precious Metals, Inc.. The 510(k) number is K904467.

When did ARGILITE 3 receive FDA 510(k) clearance?

ARGILITE 3 received FDA 510(k) clearance on 1990-10-31, under 510(k) number K904467.

Who is the listed applicant for ARGILITE 3?

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 ARGILITE 3?

The FDA product code for ARGILITE 3 is EIT.

Related Clinical Trials

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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

View all 217 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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