510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901001Substantially Equivalent

Uric Acid Test Kit

Elite Technology, Inc., Canada M9w 5p1, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901001 is the FDA 510(k) clearance record for URIC ACID TEST KIT, a class I device, cleared for Elite Technology, Inc. on under FDA product code KNK (Acid, Uric, Uricase (Colorimetric)). FDA records list 5 510(k) clearances for Elite Technology, Inc., from to . As of , FDA records show no recalls naming K901001.

Clearance record

Decision date
Received
(82 days to decision)
Product code
KNK Acid, Uric, Uricase (Colorimetric)
Regulation
21 CFR 862.1775
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Elite Technology, Inc. #1 - 57 Galaxy Blvd., Canada M9w 5p1, CA
Third party review
No

Clearances, product code KNK

Trailing 12 months

FDA records hold no clearances under product code KNK in the trailing twelve months.

FDA records show no clearances under product code KNK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KNK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260