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Spectralmd, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K163339
SPECTRALMD DEEPVIEW WOUND IMAGING SYSTEM 2.0
August 17, 2017
K124049
DEEPVIEW DIGITAL VIDEO PHYSIOLOGICAL PORTABLE IMAGING SYSTEM
April 18, 2013