510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K862577Substantially Equivalent

Linen (Huck) Towel

Dimed, Intl., Plant City FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862577 is the FDA 510(k) clearance record for LINEN (HUCK) TOWEL, a class II device, cleared for Dimed, Intl. on under FDA product code KKX (Drape, Surgical, Antimicrobial). FDA's definition for product code KKX reads: "Surgical drapes with an antimicrobial agent are subject to 510(k) review, under the procedures established by the 21st Century Cures Act. This product code is the class II non-exempt counterpart of PUI". FDA records list 3 510(k) clearances for Dimed, Intl., from to . As of , FDA records show no recalls naming K862577.

Clearance record

Decision date
Received
(16 days to decision)
Product code
KKX Drape, Surgical, Antimicrobial
Regulation
21 CFR 878.4370
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Dimed, Intl. 3108 Bruton Rd., Plant City FL
Third party review
No

Clearances, product code KKX

Trailing 12 months

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

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