ZIKV Detect 2.0 IgM Capture ELISA— 510(k) DEN180069
UnknownInBios International, Inc.
FDA 510(k) clearance DEN180069 for ZIKV Detect 2.0 IgM Capture ELISA, Unknown on 2019-05-23. Applicant: InBios International, Inc.. Device class: 2.
Clearance details
- Applicant
- InBios International, Inc.
- Product code
- Code QFO
- Device class
- Class 2
- Regulation
- 21 CFR 866.3935
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Seattle, WA, US
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More clearances from InBios International, Inc.
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