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BAYLIS PAIN MANAGEMENT GENERATOR MODEL: PMG-115 (FOR DOMESTIC USE), PMG-230 (FOR INTERNATIONAL USE)

Page Type
Cleared 510(K)
510(k) Number
K002565
510(k) Type
Traditional
Applicant
BAYLIS MEDICAL CO., INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/3/2001
Days to Decision
259 days
Submission Type
Statement

BAYLIS PAIN MANAGEMENT GENERATOR MODEL: PMG-115 (FOR DOMESTIC USE), PMG-230 (FOR INTERNATIONAL USE)

Page Type
Cleared 510(K)
510(k) Number
K002565
510(k) Type
Traditional
Applicant
BAYLIS MEDICAL CO., INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/3/2001
Days to Decision
259 days
Submission Type
Statement