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SmartLinx Vitals Plus Patient Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K183638
510(k) Type
Special
Applicant
Capsule Technologie
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2019
Days to Decision
112 days
Submission Type
Summary

SmartLinx Vitals Plus Patient Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K183638
510(k) Type
Special
Applicant
Capsule Technologie
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2019
Days to Decision
112 days
Submission Type
Summary