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DEMASQ IMAGING SPFTWARE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K090481
510(k) Type
Traditional
Applicant
DEMASQ LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/19/2009
Days to Decision
23 days
Submission Type
Summary

DEMASQ IMAGING SPFTWARE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K090481
510(k) Type
Traditional
Applicant
DEMASQ LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/19/2009
Days to Decision
23 days
Submission Type
Summary