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FDA 510(k)

TOPCAST

K-Number: K903550 · 1990-08-29

ApplicantArgen Precious Metals, Inc.
Decision Date1990-08-29
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOPCAST 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 1990-08-29 under 510(k) number K903550. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOPCAST?

TOPCAST is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Argen Precious Metals, Inc.. The 510(k) number is K903550.

When did TOPCAST receive FDA 510(k) clearance?

TOPCAST received FDA 510(k) clearance on 1990-08-29, under 510(k) number K903550.

Who is the listed applicant for TOPCAST?

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 TOPCAST?

The FDA product code for TOPCAST is EJT.

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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.

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Related Devices (Code: EJT)

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.

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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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