Philips CS770 IntelliSpace Critical Care and Anesthesia— 510(k) K151366

Substantially Equivalent

Philips Medical Systems

FDA 510(k) clearance K151366 for Philips CS770 IntelliSpace Critical Care and Anesthesia, Substantially Equivalent on 2015-10-30. Applicant: Philips Medical Systems.

Clearance details

Applicant
Philips Medical Systems
Product code
Code DXJ
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Andover, MA, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code DXJ

product code DXJ
Death
2
Total
2

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 →

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