Last synced on 14 November 2025 at 11:06 pm

KLS Martin Individual Patient Solutions

Page Type
Cleared 510(K)
510(k) Number
K163579
510(k) Type
Traditional
Applicant
KLS Martin LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2017
Days to Decision
336 days
Submission Type
Summary

KLS Martin Individual Patient Solutions

Page Type
Cleared 510(K)
510(k) Number
K163579
510(k) Type
Traditional
Applicant
KLS Martin LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2017
Days to Decision
336 days
Submission Type
Summary