510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K852829Substantially Equivalent

Cardisuny 501 a

Atrix, Portland OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852829 is the FDA 510(k) clearance record for CARDISUNY 501 A, a class II device, cleared for Atrix on under FDA product code DPS (Electrocardiograph). FDA records list 2 510(k) clearances for Atrix, from to . As of , FDA records show no recalls naming K852829.

Clearance record

Decision date
Received
(238 days to decision)
Product code
DPS Electrocardiograph
Regulation
21 CFR 870.2340
Device class
Class II
Review panel
Cardiovascular
Applicant
Atrix 1616 SW Sunset, Suite H, Portland OR
Third party review
No

Clearances, product code DPS

Trailing 12 months
6 clearances under product code DPS in the twelve months to October 2026, September 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DPS, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20262
October 20260