CL DETECT RAPID TEST— 510(k) K141341
Substantially EquivalentInBios International, Inc.
FDA 510(k) clearance K141341 for CL DETECT RAPID TEST, Substantially Equivalent on 2014-11-14. Applicant: InBios International, Inc..
Clearance details
- Applicant
- InBios International, Inc.
- Product code
- Code PIT
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Seattle, WA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.