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POLY-TECH ANGIOGRAPHY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862030
510(k) Type
Traditional
Applicant
POLY-TECH MEDICAL DEVICE RESEARCH & DEVELOPMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1986
Days to Decision
72 days

POLY-TECH ANGIOGRAPHY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862030
510(k) Type
Traditional
Applicant
POLY-TECH MEDICAL DEVICE RESEARCH & DEVELOPMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1986
Days to Decision
72 days