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SmartLinx Vitals Plus Patient Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K180734
510(k) Type
Traditional
Applicant
Capsule Technologie
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2018
Days to Decision
141 days
Submission Type
Summary

SmartLinx Vitals Plus Patient Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K180734
510(k) Type
Traditional
Applicant
Capsule Technologie
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2018
Days to Decision
141 days
Submission Type
Summary