Last synced on 25 January 2026 at 3:41 am

JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051827
510(k) Type
Traditional
Applicant
Joimax GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2005
Days to Decision
37 days
Submission Type
Summary

JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051827
510(k) Type
Traditional
Applicant
Joimax GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2005
Days to Decision
37 days
Submission Type
Summary