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Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193343
510(k) Type
Traditional
Applicant
VitalConnect, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2020
Days to Decision
139 days
Submission Type
Summary

Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193343
510(k) Type
Traditional
Applicant
VitalConnect, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2020
Days to Decision
139 days
Submission Type
Summary