AutoChamber— 510(k) K240786
Substantially EquivalentHeartLung Corporation
FDA 510(k) clearance K240786 for AutoChamber, Substantially Equivalent on 2024-10-10. Applicant: HeartLung Corporation. Device class: 2.
Clearance details
- Applicant
- HeartLung Corporation
- Product code
- Code QIH
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
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