Last synced on 14 November 2025 at 11:06 pm

JKH Stimulator Plus

Page Type
Cleared 510(K)
510(k) Number
K182203
510(k) Type
Traditional
Applicant
JKH USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2019
Days to Decision
211 days
Submission Type
Summary

JKH Stimulator Plus

Page Type
Cleared 510(K)
510(k) Number
K182203
510(k) Type
Traditional
Applicant
JKH USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2019
Days to Decision
211 days
Submission Type
Summary