Last synced on 25 January 2026 at 3:41 am

PERIPATCH SHEET, MODELS 1.5P8, 4P4, 4P6, 6P8, 10P16, 1.5P16

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031948
510(k) Type
Traditional
Applicant
Pm Devices, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/16/2003
Days to Decision
84 days
Submission Type
Statement

PERIPATCH SHEET, MODELS 1.5P8, 4P4, 4P6, 6P8, 10P16, 1.5P16

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031948
510(k) Type
Traditional
Applicant
Pm Devices, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/16/2003
Days to Decision
84 days
Submission Type
Statement