Active Anthrax DetectTM Plus Rapid Test— 510(k) DEN220044

Name: FDA 510(k) clearance DEN220044
Creator: U.S. Food and Drug Administration
Published: 2023-02-03

Unknown

InBios International, Inc.

FDA 510(k) clearance DEN220044 for Active Anthrax DetectTM Plus Rapid Test, Unknown on 2023-02-03. Applicant: InBios International, Inc.. Device class: 2.

Clearance details

Applicant: InBios International, Inc.
Product code: Code QUU
Device class: Class 2
Regulation: 21 CFR 866.3046
Advisory panel: Microbiology
Date received: 2022-07-08
Decision date: 2023-02-03
Decision: Unknown
Clearance type: Direct
Location: Seattle, WA, US

View on FDA.gov ↗

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