510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930501Substantially Equivalent

Du Pont Aca Nev/eev Verifier

Dupont Medical Products, Wilmington DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930501 is the FDA 510(k) clearance record for DU PONT ACA NEV/EEV VERIFIER, a class II device, cleared for Dupont Medical Products on under FDA product code JIS (Calibrator, Primary). FDA records list 28 510(k) clearances for Dupont Medical Products, from to . As of , FDA records show no recalls naming K930501.

Clearance record

Decision date
Received
(189 days to decision)
Product code
JIS Calibrator, Primary
Regulation
21 CFR 862.1150
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Dupont Medical Products Bmp 22/1168, Wilmington DE
510(k) summary
Summary
Third party review
No

Clearances, product code JIS

Trailing 12 months

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

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