Altris IMS— 510(k) K232088
Substantially EquivalentAltris, Inc.
FDA 510(k) clearance K232088 for Altris IMS, Substantially Equivalent on 2023-07-31. Applicant: Altris, Inc.. Device class: 2.
Clearance details
- Applicant
- Altris, Inc.
- Product code
- Code NFJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
Recent devices under product code NFJ
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