510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K110103Substantially Equivalent

Edwards Lifesciences Left Atrial Pressure Monitor Catheter

Edwards Lifesciences LLC, Draper UT / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110103 is the FDA 510(k) clearance record for EDWARDS LIFESCIENCES LEFT ATRIAL PRESSURE MONITOR CATHETER, a class II device, cleared for Edwards Lifesciences, LLC on under FDA product code DQO (Catheter, Intravascular, Diagnostic). FDA records list 165 510(k) clearances for Edwards Lifesciences, LLC, from to . As of , FDA records show no recalls naming K110103.

Clearance record

Decision date
Received
(29 days to decision)
Product code
DQO Catheter, Intravascular, Diagnostic
Regulation
21 CFR 870.1200
Device class
Class II
Review panel
Cardiovascular
Applicant
Edwards Lifesciences, LLC 12050 Lone Peak Pkwy., Draper UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQO

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