DeviceClearance

INTELLISPACE ECG— 510(k) K120855

Substantially Equivalent

Philips Health Care

FDA 510(k) clearance K120855 for INTELLISPACE ECG, Substantially Equivalent on 2012-06-29. Applicant: Philips Health Care. Device class: 2.

Clearance details

Applicant
Philips Health Care
Product code
Code DQK
Device class
Class 2
Regulation
21 CFR 870.1425
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Thousand Oaks, CA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code DQK

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Adverse events under product code DQK

product code DQK
Death
10
Injury
225
Malfunction
2,123
Other
2
Total
2,360

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 K120855

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 K120855.

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