FDA 510(k)

MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE

K-Number: K833394 · 1983-11-03

Decision Date1983-11-03

Product CodeKIT

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE 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 1983-11-03 under 510(k) number K833394. 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 MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE?

MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Sigma Chemical Co.. The 510(k) number is K833394.

When did MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE receive FDA 510(k) clearance?

MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE received FDA 510(k) clearance on 1983-11-03, under 510(k) number K833394.

Who is the listed applicant for MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE?

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 MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE?

The FDA product code for MEDIUM 199 W/HANK'S SALT W/L-GLUTAMINE is KIT.

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Other records listing Sigma Chemical Co. as applicant

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Related Devices (Code: KIT)

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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.