Active Anthrax DetectTM Plus Rapid Test— 510(k) DEN220044
UnknownInBios International, Inc.
FDA 510(k) clearance DEN220044 for Active Anthrax DetectTM Plus Rapid Test, Unknown on 2023-02-03. Applicant: InBios International, Inc..
Clearance details
- Applicant
- InBios International, Inc.
- Product code
- Code QUU
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Seattle, WA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.