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BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002389
510(k) Type
Traditional
Applicant
BAYLIS MEDICAL CO., INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/23/2000
Days to Decision
80 days
Submission Type
Statement

BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002389
510(k) Type
Traditional
Applicant
BAYLIS MEDICAL CO., INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/23/2000
Days to Decision
80 days
Submission Type
Statement