Philips Electronics Nederland B.V.

FDA Regulatory Profile

Philips Electronics Nederland B.V. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 20, 2019.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K192259Philips IntelliSite Pathology SolutionSeptember 20, 2019
K171055Philips BlueControlJuly 6, 2017