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Endiscope, Endiscope Cervical

Page Type
Cleared 510(K)
510(k) Number
K180766
510(k) Type
Traditional
Applicant
Elliquence, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2018
Days to Decision
80 days
Submission Type
Summary

Endiscope, Endiscope Cervical

Page Type
Cleared 510(K)
510(k) Number
K180766
510(k) Type
Traditional
Applicant
Elliquence, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2018
Days to Decision
80 days
Submission Type
Summary