FDA 510(k)

URIC ACID STANDARD

K-Number: K792046 · 1979-10-30

Decision Date1979-10-30

Product CodeJIS

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

URIC ACID STANDARD is the device name listed in this FDA 510(k) record. The listed applicant is Gilford Diagnostics. It received FDA 510(k) clearance on 1979-10-30 under 510(k) number K792046. 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 STANDARD?

URIC ACID STANDARD is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is Gilford Diagnostics. The 510(k) number is K792046.

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

URIC ACID STANDARD received FDA 510(k) clearance on 1979-10-30, under 510(k) number K792046.

Who is the listed applicant for URIC ACID STANDARD?

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

What is the FDA product code for URIC ACID STANDARD?

The FDA product code for URIC ACID STANDARD is JIS.

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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.