Last synced on 19 July 2024 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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