URIC ACID REAGENT— 510(k) K791754

Substantially Equivalent

Gilford Diagnostics

FDA 510(k) clearance K791754 for URIC ACID REAGENT, Substantially Equivalent on 1979-09-27. Applicant: Gilford Diagnostics. Device class: 1.

Clearance details

Applicant
Gilford Diagnostics
Product code
Code KNK
Device class
Class 1
Regulation
21 CFR 862.1775
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code KNK

view all

More clearances from Gilford Diagnostics

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.