510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913047Substantially Equivalent

Sterilesert(tm) Cable and Pole Drape

Arch Development Group, St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913047 is the FDA 510(k) clearance record for STERILESERT(TM) CABLE AND POLE DRAPE, a class II device, cleared for Arch Development Group 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 2 510(k) clearances for Arch Development Group, from to . As of , FDA records show no recalls naming K913047.

Clearance record

Decision date
Received
(85 days to decision)
Product code
KKX Drape, Surgical, Antimicrobial
Regulation
21 CFR 878.4370
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Arch Development Group 9648 Olive Blvd., Suite 411, St. Louis MO
510(k) summary
Statement
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