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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

Carescape Canvas 1000; Carescape Canvas Smart Display

FDA 510(k) source

510(k) number
K260343
Applicant
GE Healthcare Finland Oy
Decision date
Aug 28, 2026
Date received
Feb 2, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
MHX
Device type
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Device class
Class II
Regulation
21 CFR 870.1025
Advisory committee
Cardiovascular
Statement or summary
Summary
Third party
N
Location
Helsinki, FI