(DMF/F-12) HYBRI-MAX(TM) W/L-GLUTAMINE
K-Number: K871191 · 1987-04-03
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Device Summary
Frequently Asked Questions
What is the (DMF/F-12) HYBRI-MAX(TM) W/L-GLUTAMINE?
(DMF/F-12) HYBRI-MAX(TM) W/L-GLUTAMINE is a medical device that received FDA 510(k) clearance on 1987-04-03. The listed applicant is Sigma Chemical Co.. The 510(k) number is K871191.
When did (DMF/F-12) HYBRI-MAX(TM) W/L-GLUTAMINE receive FDA 510(k) clearance?
(DMF/F-12) HYBRI-MAX(TM) W/L-GLUTAMINE received FDA 510(k) clearance on 1987-04-03, under 510(k) number K871191.
Who is the listed applicant for (DMF/F-12) HYBRI-MAX(TM) 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 (DMF/F-12) HYBRI-MAX(TM) W/L-GLUTAMINE?
The FDA product code for (DMF/F-12) HYBRI-MAX(TM) W/L-GLUTAMINE 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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