VISIONAIR— 510(k) K221892
Substantially EquivalentPacificmd Biotech, LLC
FDA 510(k) clearance K221892 for VISIONAIR, Substantially Equivalent on 2022-10-05. Applicant: Pacificmd Biotech, LLC. Device class: 2.
Clearance details
- Applicant
- Pacificmd Biotech, LLC
- Product code
- Code BXQ
- Device class
- Class 2
- Regulation
- 21 CFR 868.1800
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Henderson, NV, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.