510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920867Substantially Equivalent

Eme Mp3000 Monitoring and Diagnostic Resting ECG

Electro Medical Equipment Co., Inc., Baton Rouge LA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920867 is the FDA 510(k) clearance record for EME MP3000 MONITORING AND DIAGNOSTIC RESTING ECG, a class II device, cleared for Electro Medical Equipment Co., Inc. on under FDA product code DRX (Electrode, Electrocardiograph). FDA records list one 510(k) clearance for Electro Medical Equipment Co., Inc. As of , FDA records show no recalls naming K920867.

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
Electro Medical Equipment Co., Inc. 2266 Riverside N., Baton Rouge LA
510(k) summary
Statement
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 October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DRX, 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