CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, CARESCAPE Canvas D19, F2 Frame (F2-01)— 510(k) K223531

Substantially Equivalent

GE Healthcare Finland Oy

FDA 510(k) clearance K223531 for CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, CARESCAPE Canvas D19, F2 Frame (F2-01), Substantially Equivalent on 2023-04-06. Applicant: GE Healthcare Finland Oy. Device class: 2.

Clearance details

Applicant
GE Healthcare Finland Oy
Product code
Code MHX
Device class
Class 2
Regulation
21 CFR 870.1025
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Helsinki, FI
Download summary PDFView on FDA.gov ↗

Recent devices under product code MHX

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More clearances from GE Healthcare Finland Oy

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Adverse events under product code MHX

product code MHX
Death
580
Injury
2,441
Malfunction
12,655
Other
3
Total
15,679

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K223531

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K223531.

Data sourced from openFDA. This site is unofficial and independent of the FDA.