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BAYLIS PAIN MANAGEMENT GENERATOR (PMG), MODELS PMG-115 (DOMESTIC), PMG-230 (INTERNATIONAL)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020354
510(k) Type
Traditional
Applicant
BAYLIS MEDICAL CO., INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/3/2002
Days to Decision
88 days
Submission Type
Statement

BAYLIS PAIN MANAGEMENT GENERATOR (PMG), MODELS PMG-115 (DOMESTIC), PMG-230 (INTERNATIONAL)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020354
510(k) Type
Traditional
Applicant
BAYLIS MEDICAL CO., INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/3/2002
Days to Decision
88 days
Submission Type
Statement