510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K862473Substantially Equivalent

Pdq Amebiasis

Diamedix Corp., Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862473 is the FDA 510(k) clearance record for PDQ AMEBIASIS, a class II device, cleared for Diamedix Corp. on under FDA product code KHW (Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.). FDA records list 68 510(k) clearances for Diamedix Corp., from to . As of , FDA records show no recalls naming K862473.

Clearance record

Decision date
Received
(32 days to decision)
Product code
KHW Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.
Regulation
21 CFR 866.3220
Device class
Class II
Review panel
Microbiology
Applicant
Diamedix Corp. 2140 N. Miami Ave., Miami FL
Third party review
No

Clearances, product code KHW

Trailing 12 months

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

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