510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K091856Substantially Equivalent

Conmed ECG Monitoring Electrodes , Model 1700 ( Including 2500), 1750, 2700, 2710, 1800, Series

ConMed Corporation, Utica NY / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K091856 is the FDA 510(k) clearance record for CONMED ECG MONITORING ELECTRODES , MODEL 1700 ( INCLUDING 2500), 1750, 2700, 2710, 1800, SERIES, a class II device, cleared for Conmed Corporation on under FDA product code DRX (Electrode, Electrocardiograph). FDA records list 84 510(k) clearances for Conmed Corporation, from to . As of , FDA records show no recalls naming K091856.

Clearance record

Decision date
Received
(45 days to decision)
Product code
DRX Electrode, Electrocardiograph
Regulation
21 CFR 870.2360
Device class
Class II
Review panel
Cardiovascular
Applicant
Conmed Corporation 525 French Rd., Utica NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DRX

Trailing 12 months

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

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