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3 CHANNEL DIGITAL AMBULATORY ECG RECORDER MODEL GALIX GBI-3SM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092853
510(k) Type
Traditional
Applicant
GALIX BIOMEDICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2010
Days to Decision
296 days
Submission Type
Statement

3 CHANNEL DIGITAL AMBULATORY ECG RECORDER MODEL GALIX GBI-3SM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092853
510(k) Type
Traditional
Applicant
GALIX BIOMEDICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2010
Days to Decision
296 days
Submission Type
Statement