Last synced on 14 November 2025 at 11:06 pm

SonoPlex STIM; SonoPlex II

Page Type
Cleared 510(K)
510(k) Number
K243682
510(k) Type
Traditional
Applicant
PAJUNK GmbH Medizintechnologie
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/27/2025
Days to Decision
210 days
Submission Type
Summary

SonoPlex STIM; SonoPlex II

Page Type
Cleared 510(K)
510(k) Number
K243682
510(k) Type
Traditional
Applicant
PAJUNK GmbH Medizintechnologie
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/27/2025
Days to Decision
210 days
Submission Type
Summary