IQ-UIP— 510(k) K242467
Substantially EquivalentImbio, Inc.
FDA 510(k) clearance K242467 for IQ-UIP, Substantially Equivalent on 2024-12-19. Applicant: Imbio, Inc.. Device class: 2.
Clearance details
- Applicant
- Imbio, Inc.
- Product code
- Code QWO
- Device class
- Class 2
- Regulation
- 21 CFR 892.2085
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
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