Last synced on 14 November 2025 at 11:06 pm

CORDIS VENTRICULAR ANTECHAMBER (VA)

Page Type
Cleared 510(K)
510(k) Number
K955832
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1996
Days to Decision
90 days
Submission Type
Summary

CORDIS VENTRICULAR ANTECHAMBER (VA)

Page Type
Cleared 510(K)
510(k) Number
K955832
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1996
Days to Decision
90 days
Submission Type
Summary