Analytic for Hemodynamic Instability (AHI)— 510(k) DEN200022
UnknownFifth Eye, Inc.
FDA 510(k) clearance DEN200022 for Analytic for Hemodynamic Instability (AHI), Unknown on 2021-03-01. Applicant: Fifth Eye, Inc.. Device class: 2.
Clearance details
- Applicant
- Fifth Eye, Inc.
- Product code
- Code QNV
- Device class
- Class 2
- Regulation
- 21 CFR 870.2220
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Ann Arbor, MI, US
Recent devices under product code QNV
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