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FDA 510(k)

UV URIC ACID DETERMINATION

K-Number: K790834 · 1979-06-28

ApplicantThe Dow Chemical Co.
Decision Date1979-06-28
Product CodeCDO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UV URIC ACID DETERMINATION is the device name listed in this FDA 510(k) record. The listed applicant is The Dow Chemical Co.. It received FDA 510(k) clearance on 1979-06-28 under 510(k) number K790834. The device is classified under product code CDO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UV URIC ACID DETERMINATION?

UV URIC ACID DETERMINATION is a medical device that received FDA 510(k) clearance on 1979-06-28. The listed applicant is The Dow Chemical Co.. The 510(k) number is K790834.

When did UV URIC ACID DETERMINATION receive FDA 510(k) clearance?

UV URIC ACID DETERMINATION received FDA 510(k) clearance on 1979-06-28, under 510(k) number K790834.

Who is the listed applicant for UV URIC ACID DETERMINATION?

The FDA 510(k) record lists The Dow Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UV URIC ACID DETERMINATION?

The FDA product code for UV URIC ACID DETERMINATION is CDO.

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Other records listing The Dow 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.

K823474ENZYMATIC GLUCOSE DETERMINATIONK822154UREA NITROGEN (ENZYMATIC) DETERMINATIONK821536DOWFLOW ALT-UV DETERMINATIONK821315DOWFLOW ENZYMATIC TRIGLYCERIDES DETERMK820675BILIRUBIN(TOTAL) DETERMINATION CTMSK820714DOW BILIRUBIN(DIRECT) DETERMINATION

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Related Devices (Code: CDO)

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.

K033278RANDOX URIC ACIDRandox Laboratories, Ltd.K992798SIGMA DIAGNOSTICS INFINITY URIC ACID REAGENT, MODELS 684-25, 684-100P, 684-500P, 684-2000P, 683-20, 683-100PSigma Diagnostics, Inc.K982251SIGMA DIAGNOSTICS INFINITY URIC ACID REAGENT KITSigma Diagnostics, Inc.K981766URIC ACIDAbbott LaboratoriesK981189URIC ACIDAbbott LaboratoriesK971485URIC ACID - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)Trace America, Inc.

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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