VORTRAN APM-Plus— 510(k) K182292
Substantially EquivalentVortran Medical Technology 1, Inc.
FDA 510(k) clearance K182292 for VORTRAN APM-Plus, Substantially Equivalent on 2019-09-18. Applicant: Vortran Medical Technology 1, Inc.. Device class: 2.
Clearance details
- Applicant
- Vortran Medical Technology 1, Inc.
- Product code
- Code CAP
- Device class
- Class 2
- Regulation
- 21 CFR 868.2600
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sacramento, CA, US
Recent devices under product code CAP
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