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FDA 510(k)

MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB

K-Number: K842775 · 1984-08-17

Decision Date1984-08-17
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB 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 1984-08-17 under 510(k) number K842775. 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 MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB?

MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Sigma Chemical Co.. The 510(k) number is K842775.

When did MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB receive FDA 510(k) clearance?

MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842775.

Who is the listed applicant for MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB?

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 MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB?

The FDA product code for MIN. ESSENTIAL MED. W/L-GLUTAMINE, RIB 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.

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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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