Last synced on 14 June 2024 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040835
510(k) Type
Traditional
Applicant
PM DEVICES, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/15/2004
Days to Decision
76 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040835
510(k) Type
Traditional
Applicant
PM DEVICES, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/15/2004
Days to Decision
76 days
Submission Type
Summary