FDA 510(k)

WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125

K-Number: K870483 · 1987-03-30

Decision Date1987-03-30

Product CodeKIT

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125 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 1987-03-30 under 510(k) number K870483. 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 WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125?

WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125 is a medical device that received FDA 510(k) clearance on 1987-03-30. The listed applicant is Sigma Chemical Co.. The 510(k) number is K870483.

When did WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125 receive FDA 510(k) clearance?

WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125 received FDA 510(k) clearance on 1987-03-30, under 510(k) number K870483.

Who is the listed applicant for WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125?

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 WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125?

The FDA product code for WILLIAMS' MEDIUM E W/L-GLUTAMINE #W4125 is KIT.

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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.