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DANTEC MONOPOLAR LUMEN ELECTRODE (13R18 AND 13R19)

Page Type
Cleared 510(K)
510(k) Number
K950314
510(k) Type
Traditional
Applicant
Dantec Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1996
Days to Decision
424 days
Submission Type
Statement

DANTEC MONOPOLAR LUMEN ELECTRODE (13R18 AND 13R19)

Page Type
Cleared 510(K)
510(k) Number
K950314
510(k) Type
Traditional
Applicant
Dantec Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1996
Days to Decision
424 days
Submission Type
Statement