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MODIFICATION TO CARDEON ASCENDING BALLOON CANNULA (ABC)

Page Type
Cleared 510(K)
510(k) Number
K022042
510(k) Type
Traditional
Applicant
CARDEON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2002
Days to Decision
71 days
Submission Type
Summary

MODIFICATION TO CARDEON ASCENDING BALLOON CANNULA (ABC)

Page Type
Cleared 510(K)
510(k) Number
K022042
510(k) Type
Traditional
Applicant
CARDEON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2002
Days to Decision
71 days
Submission Type
Summary