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VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003551
510(k) Type
Traditional
Applicant
JOSTRA AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2001
Days to Decision
236 days
Submission Type
Summary

VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003551
510(k) Type
Traditional
Applicant
JOSTRA AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2001
Days to Decision
236 days
Submission Type
Summary