ARGOSY DYNAMEQ
K-Number: K971699 · 1997-07-03
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Device Summary
Frequently Asked Questions
What is the ARGOSY DYNAMEQ?
ARGOSY DYNAMEQ is a medical device that received FDA 510(k) clearance on 1997-07-03. The listed applicant is Argosy Electronics. The 510(k) number is K971699.
When did ARGOSY DYNAMEQ receive FDA 510(k) clearance?
ARGOSY DYNAMEQ received FDA 510(k) clearance on 1997-07-03, under 510(k) number K971699.
Who is the listed applicant for ARGOSY DYNAMEQ?
The FDA 510(k) record lists Argosy Electronics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARGOSY DYNAMEQ?
The FDA product code for ARGOSY DYNAMEQ is ESD.
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 Argosy Electronics 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: ESD)
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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