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FDA 510(k)

CENTRIFICHEM URIC ACID

K-Number: K800130 · 1980-02-13

Decision Date1980-02-13
Product CodeCDO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIFICHEM URIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1980-02-13 under 510(k) number K800130. 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 CENTRIFICHEM URIC ACID?

CENTRIFICHEM URIC ACID is a medical device that received FDA 510(k) clearance on 1980-02-13. The listed applicant is Union Carbide Corp.. The 510(k) number is K800130.

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

CENTRIFICHEM URIC ACID received FDA 510(k) clearance on 1980-02-13, under 510(k) number K800130.

Who is the listed applicant for CENTRIFICHEM URIC ACID?

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

What is the FDA product code for CENTRIFICHEM URIC ACID?

The FDA product code for CENTRIFICHEM URIC ACID is CDO.

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 Union Carbide 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 69 devices →

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.

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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