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FDA 510(k)

URIC ACID STD. FOR QUANT. URIC ACID

K-Number: K772025 · 1977-11-11

Decision Date1977-11-11
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID STD. FOR QUANT. URIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Worthington Biochemical Corp.. It received FDA 510(k) clearance on 1977-11-11 under 510(k) number K772025. 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 URIC ACID STD. FOR QUANT. URIC ACID?

URIC ACID STD. FOR QUANT. URIC ACID is a medical device that received FDA 510(k) clearance on 1977-11-11. The listed applicant is Worthington Biochemical Corp.. The 510(k) number is K772025.

When did URIC ACID STD. FOR QUANT. URIC ACID receive FDA 510(k) clearance?

URIC ACID STD. FOR QUANT. URIC ACID received FDA 510(k) clearance on 1977-11-11, under 510(k) number K772025.

Who is the listed applicant for URIC ACID STD. FOR QUANT. URIC ACID?

The FDA 510(k) record lists Worthington Biochemical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URIC ACID STD. FOR QUANT. URIC ACID?

The FDA product code for URIC ACID STD. FOR QUANT. URIC ACID is JIS.

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 Worthington Biochemical 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.

View all 13 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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