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PERIPATCH ENDO-SLEEVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063556
510(k) Type
Traditional
Applicant
PM DEVICES, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/20/2007
Days to Decision
113 days
Submission Type
Statement

PERIPATCH ENDO-SLEEVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063556
510(k) Type
Traditional
Applicant
PM DEVICES, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/20/2007
Days to Decision
113 days
Submission Type
Statement