EUGONIC AGAR
K-Number: K834206 · 1984-01-03
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Device Summary
Frequently Asked Questions
What is the EUGONIC AGAR?
EUGONIC AGAR is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K834206.
When did EUGONIC AGAR receive FDA 510(k) clearance?
EUGONIC AGAR received FDA 510(k) clearance on 1984-01-03, under 510(k) number K834206.
Who is the listed applicant for EUGONIC AGAR?
The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EUGONIC AGAR?
The FDA product code for EUGONIC AGAR is JSG.
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 Acumedia Manufacturers, 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: JSG)
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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