510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K013624Substantially Equivalent

Modification to Agilent Component Monitoring System (Cms), V24/v26 Patient Monitors, Blood Analysis Portal System Plug-I

Philips Medizin Systeme Boblingen GmbH, Andover MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K013624 is the FDA 510(k) clearance record for MODIFICATION TO AGILENT COMPONENT MONITORING SYSTEM (CMS), V24/V26 PATIENT MONITORS, BLOOD ANALYSIS PORTAL SYSTEM PLUG-I, a class II device, cleared for Philips Medizin Systeme Boblingen GmbH on under FDA product code MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)). FDA records list 22 510(k) clearances for Philips Medizin Systeme Boblingen GmbH, from to . As of , FDA records show no recalls naming K013624.

Clearance record

Decision date
Received
(28 days to decision)
Product code
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Regulation
21 CFR 870.1025
Device class
Class II
Review panel
Cardiovascular
Applicant
Philips Medizin Systeme Boblingen GmbH 3000 Minuteman Rd., Andover MA
510(k) summary
Summary
Third party review
No

Clearances, product code MHX

Trailing 12 months
15 clearances under product code MHX in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code MHX, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20261
March 20260
April 20263
May 20262
June 20261
July 20261
August 20263
September 20261
October 20260