Last synced on 25 April 2025 at 11:05 pm

CARDIOTRON EKG MULTI-PHASE INFORMATION ANALYSIS SYSTEM, MODELS 3800, 6800, 8800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992703
510(k) Type
Traditional
Applicant
PREMIER HEART, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2000
Days to Decision
222 days
Submission Type
Summary

CARDIOTRON EKG MULTI-PHASE INFORMATION ANALYSIS SYSTEM, MODELS 3800, 6800, 8800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992703
510(k) Type
Traditional
Applicant
PREMIER HEART, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2000
Days to Decision
222 days
Submission Type
Summary