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MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885175
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1989
Days to Decision
212 days

MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885175
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1989
Days to Decision
212 days