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joimax Electrosurgical Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161378
510(k) Type
Traditional
Applicant
JOIMAX GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/2/2016
Days to Decision
168 days
Submission Type
Summary

joimax Electrosurgical Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161378
510(k) Type
Traditional
Applicant
JOIMAX GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/2/2016
Days to Decision
168 days
Submission Type
Summary