510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K172259Substantially Equivalent

PulsioFlex Monitoring System

Pulsion Medical Systems SE, Feldkirchen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K172259 is the FDA 510(k) clearance record for PulsioFlex Monitoring System, a class II device, cleared for Pulsion Medical Systems SE on under FDA product code DXG (Computer, Diagnostic, Pre-Programmed, Single-Function). FDA records list 4 510(k) clearances for Pulsion Medical Systems SE, from to . As of , FDA records show one recall naming K172259.

Clearance record

Decision date
Received
(175 days to decision)
Product code
DXG Computer, Diagnostic, Pre-Programmed, Single-Function
Regulation
21 CFR 870.1435
Device class
Class II
Review panel
Cardiovascular
Applicant
Pulsion Medical Systems SE Hans-Riedl-Str. 17, Feldkirchen, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DXG

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