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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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