Last synced on 30 September 2022 at 11:05 pm

PERIPATCH SLEEVE, MODELS G35, E35, G45, E45, G60, E60, 5C6, 5C8, 5C10

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033985
510(k) Type
Traditional
Applicant
PM DEVICES, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/4/2004
Days to Decision
164 days
Submission Type
Summary

PERIPATCH SLEEVE, MODELS G35, E35, G45, E45, G60, E60, 5C6, 5C8, 5C10

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033985
510(k) Type
Traditional
Applicant
PM DEVICES, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/4/2004
Days to Decision
164 days
Submission Type
Summary