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COAXIAL DUAL FLOW CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820859
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1982
Days to Decision
18 days

COAXIAL DUAL FLOW CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820859
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1982
Days to Decision
18 days