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MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS

Page Type
Cleared 510(K)
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)
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