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General Equipment For Medical Imaging (Oncovision-

FDA Regulatory Profile

General Equipment For Medical Imaging (Oncovision- appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 18, 2016.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K162052Sentinella 102, Sentinella 102 HorusAugust 18, 2016
K143156Sentinella 102; Sentinella 102 HorusNovember 18, 2014
K140996MAMMIJune 11, 2014

FDA data resources