BUN REAGENT
K-Number: K942984 · 1995-03-01
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Device Summary
Frequently Asked Questions
What is the BUN REAGENT?
BUN REAGENT is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is American Research Products Co.. The 510(k) number is K942984.
When did BUN REAGENT receive FDA 510(k) clearance?
BUN REAGENT received FDA 510(k) clearance on 1995-03-01, under 510(k) number K942984.
Who is the listed applicant for BUN REAGENT?
The FDA 510(k) record lists American Research Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BUN REAGENT?
The FDA product code for BUN REAGENT is CDQ.
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 American Research Products 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: CDQ)
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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