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VL7600 REM PATIENT RETURN ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K953737
510(k) Type
Traditional
Applicant
VALLEYLAB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/1995
Days to Decision
13 days
Submission Type
Summary

VL7600 REM PATIENT RETURN ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K953737
510(k) Type
Traditional
Applicant
VALLEYLAB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/1995
Days to Decision
13 days
Submission Type
Summary