VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B— 510(k) K900115
Substantially EquivalentVentlab Corp.
FDA 510(k) clearance K900115 for VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B, Substantially Equivalent on 1990-02-22. Applicant: Ventlab Corp.. Device class: 1.
Clearance details
- Applicant
- Ventlab Corp.
- Product code
- Code CAN
- Device class
- Class 1
- Regulation
- 21 CFR 868.2700
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hackensack, NJ, US
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Adverse events under product code CAN
product code CAN- Death
- 4
- Other
- 1
- Total
- 5
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.