Aluna— 510(k) K193311
Substantially EquivalentKnox Medical Diagnostics, Inc.
FDA 510(k) clearance K193311 for Aluna, Substantially Equivalent on 2020-03-25. Applicant: Knox Medical Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Knox Medical Diagnostics, Inc.
- Product code
- Code BZH
- Device class
- Class 2
- Regulation
- 21 CFR 868.1860
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Francisco, CA, US
Recent devices under product code BZH
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