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CRITERION, CRITERION I.V., MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952267
510(k) Type
Traditional
Applicant
NOVA-VENTRX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1997
Days to Decision
932 days
Submission Type
Statement

CRITERION, CRITERION I.V., MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952267
510(k) Type
Traditional
Applicant
NOVA-VENTRX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1997
Days to Decision
932 days
Submission Type
Statement