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joimax Electrosurgical Instruments

Page Type
Cleared 510(K)
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)
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