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SYSTEM 90 INTRA-AORTIC BALLOON PUMP CONSOLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921638
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1993
Days to Decision
310 days
Submission Type
Statement

SYSTEM 90 INTRA-AORTIC BALLOON PUMP CONSOLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921638
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1993
Days to Decision
310 days
Submission Type
Statement