510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K181726Substantially Equivalent

Medline Patient Cables and Lead Wires

MEDLINE INDUSTRIES, LP - Northfield, Northfiled IL / Traditional, Substantially Equivalent

K181726 is the FDA 510(k) clearance record for Medline Patient Cables and Lead Wires, a class II device, cleared for Medline Industries, Inc. on under FDA product code DSA (Cable, Transducer And Electrode, Patient, (Including Connector)). FDA records list 414 510(k) clearances for MEDLINE INDUSTRIES, LP - Northfield, from to . As of , FDA records show no recalls naming K181726.

Clearance record

Decision date
Received
(83 days to decision)
Product code
DSA Cable, Transducer And Electrode, Patient, (Including Connector)
Regulation
21 CFR 870.2900
Device class
Class II
Review panel
Cardiovascular
Applicant
Medline Industries, Inc. Three Lakes Dr., Northfiled IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DSA

Trailing 12 months
2 clearances under product code DSA in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DSA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260