510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980032Substantially Equivalent

Salicylate Assay (Ace), Catalogue Number 501-71

Sekisui Diagnostics P.E.I. Inc., Charlottetown, P.E.I., CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980032 is the FDA 510(k) clearance record for SALICYLATE ASSAY (ACE), CATALOGUE NUMBER 501-71, a class II device, cleared for Diagnostic Chemicals , Ltd. on under FDA product code DKJ (Colorimetry, Salicylate). FDA records list 72 510(k) clearances for Sekisui Diagnostics P.E.I. Inc., from to . As of , FDA records show no recalls naming K980032.

Clearance record

Decision date
Received
(56 days to decision)
Product code
DKJ Colorimetry, Salicylate
Regulation
21 CFR 862.3830
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Diagnostic Chemicals , Ltd. West Royalty Industrial Park,, Charlottetown, P.E.I., CA
510(k) summary
Statement
Third party review
No

Clearances, product code DKJ

Trailing 12 months

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

FDA records show no clearances under product code DKJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DKJ, 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