510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K904250Substantially Equivalent

Model 4222 Ambulatory ECG Monitor

Byrncrest Global, Inc., West Columbia TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K904250 is the FDA 510(k) clearance record for MODEL 4222 AMBULATORY ECG MONITOR, a class II device, cleared for Byrncrest Global, Inc. on under FDA product code DXH (Transmitters And Receivers, Electrocardiograph, Telephone). FDA records list one 510(k) clearance for Byrncrest Global, Inc. As of , FDA records show no recalls naming K904250.

Clearance record

Decision date
Received
(161 days to decision)
Product code
DXH Transmitters And Receivers, Electrocardiograph, Telephone
Regulation
21 CFR 870.2920
Device class
Class II
Review panel
Cardiovascular
Applicant
Byrncrest Global, Inc. P.O. Box 157, West Columbia TX
Third party review
No

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