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/ Philips Volcano
Philips Volcano
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K170133
FFR V2.5
May 26, 2017
K162418
Pioneer Plus Catheter
December 2, 2016