510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K243185Substantially Equivalent

REMI Remote EEG Monitoring System

Epitel, Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K243185 is the FDA 510(k) clearance record for REMI Remote EEG Monitoring System, a class II device, cleared for Epitel on under FDA product code OMC (Reduced- Montage Standard Electroencephalograph). FDA's definition for product code OMC reads: "Acquire, display, store, and archive electroencephalographic signals from the brain using a user-specified and/or sponsor-specified locations with a reduced array (i.e. less than < 16) of electrodes". FDA records list 5 510(k) clearances for Epitel, from to . As of , FDA records show no recalls naming K243185.

Clearance record

Decision date
Received
(172 days to decision)
Product code
OMC Reduced- Montage Standard Electroencephalograph
Regulation
21 CFR 882.1400
Device class
Class II
Review panel
Neurology
Applicant
Epitel 465 S 400 E., Salt Lake City UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OMC

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