Last synced on 20 May 2022 at 11:05 pm

MULTISTIM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011308
510(k) Type
Traditional
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2001
Days to Decision
213 days
Submission Type
Summary

MULTISTIM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011308
510(k) Type
Traditional
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2001
Days to Decision
213 days
Submission Type
Summary