Last synced on 14 November 2025 at 11:06 pm

CARDEON ASCENDING BALLOON CANNULA (ABC)

Page Type
Cleared 510(K)
510(k) Number
K001371
510(k) Type
Traditional
Applicant
CARDEON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2000
Days to Decision
67 days
Submission Type
Summary

CARDEON ASCENDING BALLOON CANNULA (ABC)

Page Type
Cleared 510(K)
510(k) Number
K001371
510(k) Type
Traditional
Applicant
CARDEON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2000
Days to Decision
67 days
Submission Type
Summary