Last synced on 14 November 2025 at 11:06 pm

PERIPATCH ENDO-SLEEVE

Page Type
Cleared 510(K)
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)
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