Last synced on 16 May 2025 at 11:05 pm

CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021694
510(k) Type
Traditional
Applicant
CARDIOVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2003
Days to Decision
231 days
Submission Type
Summary

CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021694
510(k) Type
Traditional
Applicant
CARDIOVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2003
Days to Decision
231 days
Submission Type
Summary