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SMARTDOP 30 BI-DIRECTIONAL BLOOD FLOW DETECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942613
510(k) Type
Traditional
Applicant
KOVEN TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/1994
Days to Decision
204 days
Submission Type
Statement

SMARTDOP 30 BI-DIRECTIONAL BLOOD FLOW DETECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942613
510(k) Type
Traditional
Applicant
KOVEN TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/1994
Days to Decision
204 days
Submission Type
Statement