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FDA 510(k)

MEM NON-ESSENTIAL AMINO ACIDS (100X)

K-Number: K820508 · 1982-03-26

Decision Date1982-03-26
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MEM NON-ESSENTIAL AMINO ACIDS (100X) is the device name listed in this FDA 510(k) record. The listed applicant is Dutchland Laboratories, Inc.. It received FDA 510(k) clearance on 1982-03-26 under 510(k) number K820508. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEM NON-ESSENTIAL AMINO ACIDS (100X)?

MEM NON-ESSENTIAL AMINO ACIDS (100X) is a medical device that received FDA 510(k) clearance on 1982-03-26. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K820508.

When did MEM NON-ESSENTIAL AMINO ACIDS (100X) receive FDA 510(k) clearance?

MEM NON-ESSENTIAL AMINO ACIDS (100X) received FDA 510(k) clearance on 1982-03-26, under 510(k) number K820508.

Who is the listed applicant for MEM NON-ESSENTIAL AMINO ACIDS (100X)?

The FDA 510(k) record lists Dutchland Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEM NON-ESSENTIAL AMINO ACIDS (100X)?

The FDA product code for MEM NON-ESSENTIAL AMINO ACIDS (100X) 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 Dutchland Laboratories, 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: 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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