MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDS
K-Number: K850521 · 1985-02-27
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Device Summary
Frequently Asked Questions
What is the MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDS?
MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDS is a medical device that received FDA 510(k) clearance on 1985-02-27. The listed applicant is Mediatech, Inc.. The 510(k) number is K850521.
When did MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDS receive FDA 510(k) clearance?
MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDS received FDA 510(k) clearance on 1985-02-27, under 510(k) number K850521.
Who is the listed applicant for MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDS?
The FDA 510(k) record lists Mediatech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDS?
The FDA product code for MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDS is KIT.
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 Mediatech, 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: KIT)
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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