Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K896511Substantially Equivalent

Du Pont Xenolite(tm) Radiation Protection Apparel

E.I. Dupont de Nemours & Co., Inc., Wilmington DE / Traditional, Substantially Equivalent

K896511 is the FDA 510(k) clearance record for DU PONT XENOLITE(TM) RADIATION PROTECTION APPAREL, a class I device, cleared for E.I. Dupont DE Nemours & Co., Inc. on under FDA product code KPY (Shield, Protective, Personnel). FDA records list 253 510(k) clearances for E.I. Dupont DE Nemours & Co., Inc., from to . As of , FDA records show no recalls naming K896511.

Clearance record

Decision date
Received
(38 days to decision)
Product code
KPY Shield, Protective, Personnel
Regulation
21 CFR 892.6500
Device class
Class I
Review panel
Radiology
Applicant
E.I. Dupont DE Nemours & Co., Inc. Medical Products Dept., Wilmington DE
Third party review
No

Clearances, product code KPY

Trailing 12 months

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

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