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FDA 510(k)

URIC ACID REAGENT SET

K-Number: K860111 · 1986-02-19

Decision Date1986-02-19
Product CodeLFQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID REAGENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Technostics Intl.. It received FDA 510(k) clearance on 1986-02-19 under 510(k) number K860111. The device is classified under product code LFQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URIC ACID REAGENT SET?

URIC ACID REAGENT SET is a medical device that received FDA 510(k) clearance on 1986-02-19. The listed applicant is Technostics Intl.. The 510(k) number is K860111.

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

URIC ACID REAGENT SET received FDA 510(k) clearance on 1986-02-19, under 510(k) number K860111.

Who is the listed applicant for URIC ACID REAGENT SET?

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

What is the FDA product code for URIC ACID REAGENT SET?

The FDA product code for URIC ACID REAGENT SET is LFQ.

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 Technostics Intl. 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 21 devices →

Related Devices (Code: LFQ)

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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