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MELYS ATRIAL FIBRILLATION SCREENING MONITOR

Page Type
Cleared 510(K)
510(k) Number
K132206
510(k) Type
Traditional
Applicant
ADVANCED FLUIDICS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2014
Days to Decision
246 days
Submission Type
Summary

MELYS ATRIAL FIBRILLATION SCREENING MONITOR

Page Type
Cleared 510(K)
510(k) Number
K132206
510(k) Type
Traditional
Applicant
ADVANCED FLUIDICS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2014
Days to Decision
246 days
Submission Type
Summary