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GYNEX ELECTRODES

Page Type
Cleared 510(K)
510(k) Number
K982739
510(k) Type
Traditional
Applicant
GYNEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1999
Days to Decision
218 days
Submission Type
Summary

GYNEX ELECTRODES

Page Type
Cleared 510(K)
510(k) Number
K982739
510(k) Type
Traditional
Applicant
GYNEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1999
Days to Decision
218 days
Submission Type
Summary