ARGESOL-NOVASOL
K-Number: K942943 · 1994-07-22
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Device Summary
Frequently Asked Questions
What is the ARGESOL-NOVASOL?
ARGESOL-NOVASOL is a medical device that received FDA 510(k) clearance on 1994-07-22. The listed applicant is Argen Precious Metals, Inc.. The 510(k) number is K942943.
When did ARGESOL-NOVASOL receive FDA 510(k) clearance?
ARGESOL-NOVASOL received FDA 510(k) clearance on 1994-07-22, under 510(k) number K942943.
Who is the listed applicant for ARGESOL-NOVASOL?
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 ARGESOL-NOVASOL?
The FDA product code for ARGESOL-NOVASOL is EJT.
Related Clinical Trials
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.
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.
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.
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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