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PERCOR INTRA-AORTIC BALLOON INSERTION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823342
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1983
Days to Decision
77 days

PERCOR INTRA-AORTIC BALLOON INSERTION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823342
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1983
Days to Decision
77 days