Spectralmd, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K163339SPECTRALMD DEEPVIEW WOUND IMAGING SYSTEM 2.0August 17, 2017
K124049DEEPVIEW DIGITAL VIDEO PHYSIOLOGICAL PORTABLE IMAGING SYSTEMApril 18, 2013