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VASOMEDICAL-BIOX COMBINED 12 CHANNEL AMBULATORY ECG AND BLOOD PRESSURE RECORDER MODEL 2302, VASOMEDICAL-BIOX AMBULATORY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111096
510(k) Type
Special
Applicant
VASOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2011
Days to Decision
65 days
Submission Type
Summary

VASOMEDICAL-BIOX COMBINED 12 CHANNEL AMBULATORY ECG AND BLOOD PRESSURE RECORDER MODEL 2302, VASOMEDICAL-BIOX AMBULATORY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111096
510(k) Type
Special
Applicant
VASOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2011
Days to Decision
65 days
Submission Type
Summary