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PERCOR PERCUTANEOUS INTRODUCER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820834
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1982
Days to Decision
19 days

PERCOR PERCUTANEOUS INTRODUCER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820834
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1982
Days to Decision
19 days