Last synced on 25 January 2026 at 3:41 am

Aptima Mycoplasma genitalium Assay

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN180047
510(k) Type
Direct
Applicant
Hologic, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
1/23/2019
Days to Decision
145 days

Aptima Mycoplasma genitalium Assay

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN180047
510(k) Type
Direct
Applicant
Hologic, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
1/23/2019
Days to Decision
145 days