ORTHO* CHLAMYDIA DIRECT DETECTION (FA) TEST— 510(k) K881500
Substantially EquivalentOrtho Diagnostic Systems, Inc.
FDA 510(k) clearance K881500 for ORTHO* CHLAMYDIA DIRECT DETECTION (FA) TEST, Substantially Equivalent on 1988-04-27. Applicant: Ortho Diagnostic Systems, Inc..
Clearance details
- Applicant
- Ortho Diagnostic Systems, Inc.
- Product code
- Code LJP
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Carpinteria, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.