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FDA 510(k)

UV URIC ACID STANDARDS

K-Number: K801501 · 1980-09-26

ApplicantThe Dow Chemical Co.
Decision Date1980-09-26
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UV URIC ACID STANDARDS 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 1980-09-26 under 510(k) number K801501. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UV URIC ACID STANDARDS?

UV URIC ACID STANDARDS is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is The Dow Chemical Co.. The 510(k) number is K801501.

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

UV URIC ACID STANDARDS received FDA 510(k) clearance on 1980-09-26, under 510(k) number K801501.

Who is the listed applicant for UV URIC ACID STANDARDS?

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 STANDARDS?

The FDA product code for UV URIC ACID STANDARDS is JIS.

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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: JIS)

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.

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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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