510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K001317Substantially Equivalent

Aria

Del Mar Medical Systems, LLC, Irvine CA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K001317 is the FDA 510(k) clearance record for ARIA, a class II device, cleared for Del Mar Medical Systems, LLC on under FDA product code MWJ (Electrocardiograph, Ambulatory (Without Analysis)). FDA records list 2 510(k) clearances for Del Mar Medical Systems, LLC, from to . As of , FDA records show no recalls naming K001317.

Clearance record

Decision date
Received
(86 days to decision)
Product code
MWJ Electrocardiograph, Ambulatory (Without Analysis)
Regulation
21 CFR 870.2800
Device class
Class II
Review panel
Cardiovascular
Applicant
Del Mar Medical Systems, LLC 1621 Alton Pkwy., Irvine CA
510(k) summary
Summary
Third party review
No

Clearances, product code MWJ

Trailing 12 months
5 clearances under product code MWJ in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MWJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20260
August 20261
September 20262
October 20260