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ACIST CVI1 Contrast Delivery System, A1000 Syringe Kit, A1000V Syringe Kit, BT2000 Manifold Kit, BT2000 Manifold Kit, AngioToiuch Hand Controller Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191060
510(k) Type
Traditional
Applicant
ACIST Medical Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2019
Days to Decision
87 days
Submission Type
Summary

ACIST CVI1 Contrast Delivery System, A1000 Syringe Kit, A1000V Syringe Kit, BT2000 Manifold Kit, BT2000 Manifold Kit, AngioToiuch Hand Controller Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191060
510(k) Type
Traditional
Applicant
ACIST Medical Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2019
Days to Decision
87 days
Submission Type
Summary