RAPID DIAGNOSTIC SYSTEM FOR CHLAMYDIA TRACHOMATIS— 510(k) K871878
Substantially EquivalentGen-Probe, Inc.
FDA 510(k) clearance K871878 for RAPID DIAGNOSTIC SYSTEM FOR CHLAMYDIA TRACHOMATIS, Substantially Equivalent on 1987-10-28. Applicant: Gen-Probe, Inc..
Clearance details
- Applicant
- Gen-Probe, Inc.
- Product code
- Code LSK
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.