URIC ACID REAGENT SET
K-Number: K811764 · 1981-08-20
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Device Summary
Frequently Asked Questions
What is the URIC ACID REAGENT SET?
URIC ACID REAGENT SET is a medical device that received FDA 510(k) clearance on 1981-08-20. The listed applicant is Anco Medical Reagents & Assoc.. The 510(k) number is K811764.
When did URIC ACID REAGENT SET receive FDA 510(k) clearance?
URIC ACID REAGENT SET received FDA 510(k) clearance on 1981-08-20, under 510(k) number K811764.
Who is the listed applicant for URIC ACID REAGENT SET?
The FDA 510(k) record lists Anco Medical Reagents & Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URIC ACID REAGENT SET?
The FDA product code for URIC ACID REAGENT SET is LFQ.
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 Anco Medical Reagents & Assoc. 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: LFQ)
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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