510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K042022Substantially Equivalent

E-Tac Ex-1000 Electrocardiographic Event Recorder

Datrix, Inc. dba of Jon Barron, Inc., Escondido CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K042022 is the FDA 510(k) clearance record for E-TAC EX-1000 ELECTROCARDIOGRAPHIC EVENT RECORDER, a class II device, cleared for Datrix, Inc. Dba of Jon Barron, Inc. on under FDA product code DXH (Transmitters And Receivers, Electrocardiograph, Telephone). FDA records list one 510(k) clearance for Datrix, Inc. Dba of Jon Barron, Inc. As of , FDA records show no recalls naming K042022.

Clearance record

Decision date
Received
(15 days to decision)
Product code
DXH Transmitters And Receivers, Electrocardiograph, Telephone
Regulation
21 CFR 870.2920
Device class
Class II
Review panel
Cardiovascular
Applicant
Datrix, Inc. Dba of Jon Barron, Inc. 340 State Pl., Escondido CA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code DXH

Trailing 12 months
4 clearances under product code DXH in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DXH, trailing twelve months
MonthClearances
November 20251
December 20252
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260