Last synced on 14 November 2025 at 11:06 pm

CARDEON COBRA CATHETER

Page Type
Cleared 510(K)
510(k) Number
K042156
510(k) Type
Traditional
Applicant
CARDEON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2004
Days to Decision
57 days
Submission Type
Summary

CARDEON COBRA CATHETER

Page Type
Cleared 510(K)
510(k) Number
K042156
510(k) Type
Traditional
Applicant
CARDEON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2004
Days to Decision
57 days
Submission Type
Summary