Last synced on 25 January 2026 at 3:41 am

DATASCOPE 8FR. CO-LUMEN 34 AND 40CC INTRA-AORTIC BALLOON CATHETERS FOR OPTIONAL SHEATHLESS INSERTION WITH ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980385
510(k) Type
Traditional
Applicant
Datascope Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1998
Days to Decision
88 days
Submission Type
Summary

DATASCOPE 8FR. CO-LUMEN 34 AND 40CC INTRA-AORTIC BALLOON CATHETERS FOR OPTIONAL SHEATHLESS INSERTION WITH ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980385
510(k) Type
Traditional
Applicant
Datascope Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1998
Days to Decision
88 days
Submission Type
Summary