Last synced on 14 November 2025 at 11:06 pm

Omni Hysteroscope, Omni Hysteroscope Kits, Omni Sheaths

Page Type
Cleared 510(K)
510(k) Number
K182006
510(k) Type
Special
Applicant
Hologic, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2018
Days to Decision
132 days
Submission Type
Summary

Omni Hysteroscope, Omni Hysteroscope Kits, Omni Sheaths

Page Type
Cleared 510(K)
510(k) Number
K182006
510(k) Type
Special
Applicant
Hologic, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2018
Days to Decision
132 days
Submission Type
Summary