510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K933648Substantially Equivalent

Added Use Claim for Dupont Aca Beta-2-Microglobulin Test Pack

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

K933648 is the FDA 510(k) clearance record for ADDED USE CLAIM FOR DUPONT ACA BETA-2-MICROGLOBULIN TEST PACK, a class II device, cleared for Dupont Medical Products on under FDA product code JZG (System, Test, Beta-2-Microglobulin Immunological). FDA records list 28 510(k) clearances for Dupont Medical Products, from to . As of , FDA records show no recalls naming K933648.

Clearance record

Decision date
Received
(59 days to decision)
Product code
JZG System, Test, Beta-2-Microglobulin Immunological
Regulation
21 CFR 866.5630
Device class
Class II
Review panel
Immunology
Applicant
Dupont Medical Products P.O. Box 80022, Bmp 22-1174, Wilmington DE
510(k) summary
Summary
Third party review
No

Clearances, product code JZG

Trailing 12 months

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

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