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3 CHANNEL DIGITAL AMBULATORY ECG RECORDER

Page Type
Cleared 510(K)
510(k) Number
K971670
510(k) Type
Traditional
Applicant
GALIX BIOMEDICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1998
Days to Decision
268 days
Submission Type
Statement

3 CHANNEL DIGITAL AMBULATORY ECG RECORDER

Page Type
Cleared 510(K)
510(k) Number
K971670
510(k) Type
Traditional
Applicant
GALIX BIOMEDICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1998
Days to Decision
268 days
Submission Type
Statement