G-GT REAGENT
K-Number: K851999 · 1985-06-10
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Device Summary
Frequently Asked Questions
What is the G-GT REAGENT?
G-GT REAGENT is a medical device that received FDA 510(k) clearance on 1985-06-10. The listed applicant is Alpkem Corp.. The 510(k) number is K851999.
When did G-GT REAGENT receive FDA 510(k) clearance?
G-GT REAGENT received FDA 510(k) clearance on 1985-06-10, under 510(k) number K851999.
Who is the listed applicant for G-GT REAGENT?
The FDA 510(k) record lists Alpkem Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for G-GT REAGENT?
The FDA product code for G-GT REAGENT is JQB.
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 Alpkem Corp. 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: JQB)
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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