APTIMA TRICHOMONAS VAGINALIS ASSAY— 510(k) DEN110012
UnknownGen-Probe Incorporated
FDA 510(k) clearance DEN110012 for APTIMA TRICHOMONAS VAGINALIS ASSAY, Unknown on 2011-04-19. Applicant: Gen-Probe Incorporated. Device class: 2.
Clearance details
- Applicant
- Gen-Probe Incorporated
- Product code
- Code OUY
- Device class
- Class 2
- Regulation
- 21 CFR 866.3860
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- San Diego, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.