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FDA 510(k)

MEM, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE -

K-Number: K850921 · 1985-03-25

Decision Date1985-03-25
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MEM, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE - is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1985-03-25 under 510(k) number K850921. 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, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE -?

MEM, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE - is a medical device that received FDA 510(k) clearance on 1985-03-25. The listed applicant is Sigma Chemical Co.. The 510(k) number is K850921.

When did MEM, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE - receive FDA 510(k) clearance?

MEM, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE - received FDA 510(k) clearance on 1985-03-25, under 510(k) number K850921.

Who is the listed applicant for MEM, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE -?

The FDA 510(k) record lists Sigma Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEM, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE -?

The FDA product code for MEM, M7270, W/EBSS, L-GLUTAMINE & W/O L-LEUCINE - 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 Sigma Chemical Co. 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.

View all 231 devices →

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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