510(k) K243935
- Device
- Aptima CMV Quant Assay
- Applicant
- Hologic, Inc.
- 510(k) number
- K243935
- Product code
- PAB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2025-01-17
- Date received
- 2024-12-20
- Regulation
- 866.3180
- Classification name
- Cytomegalovirus (Cmv) Dna Quantitative Assay
- Medical specialty
- Microbiology
- Review panel
- Microbiology
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- Maria Jose Cortes-Mateos
- Address
- 10210 Genetic Center Dr. San Diego CA US 92121 92121
FDA Registration Numbers#
- 2243471
- 3004141078
- 9610126
- 2024800
- 3005248192
- 3019837962
- 3025663244
- 2023365
- 3004013603
- 3003795116