Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K101596Substantially Equivalent

Kimberly-Clark Purple Nitrile Powder-Free Exam Glove (Chemotherapy Glove) and Kimberly-Clark Purple Nitrile Xtra Powder-

Kimberly-Clark Corporation, Roswell GA / Traditional, Substantially Equivalent

K101596 is the FDA 510(k) clearance record for KIMBERLY-CLARK PURPLE NITRILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) AND KIMBERLY-CLARK PURPLE NITRILE XTRA POWDER-, a class I device, cleared for Kimberly-Clark on under FDA product code LZC (Medical Glove, Specialty). FDA's definition for product code LZC reads: "A disposable medical glove (examination or surgeon’s) is a device that may or may not bear a trace amount of residual powder and is intended to be worn on the hand or finger(s) for medical purposes to prevent contamination. In addition...". FDA records list 122 510(k) clearances for Kimberly-Clark, from to . As of , FDA records show no recalls naming K101596.

Clearance record

Decision date
Received
(43 days to decision)
Product code
LZC Medical Glove, Specialty
Regulation
21 CFR 880.6250
Device class
Class I
Review panel
General Hospital
Applicant
Kimberly-Clark 1400 Holcomb Bridge Rd., Roswell GA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code LZC

Trailing 12 months
1 clearance under product code LZC in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LZC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260