Visor System— 510(k) K182967
Substantially EquivalentCerebrotech Medical Systems, Inc.
FDA 510(k) clearance K182967 for Visor System, Substantially Equivalent on 2018-11-23. Applicant: Cerebrotech Medical Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Cerebrotech Medical Systems, Inc.
- Product code
- Code QAF
- Device class
- Class 2
- Regulation
- 21 CFR 870.2770
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Pleasanton, CA, US
Recent devices under product code QAF
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