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MEDRAD Centargo CT Injection System - MEDRAD Centargo Replacement Spike
FDA 510(k)Class II (US FDA 510(k))
510(k) K241849
Identifiers
- 510(k) Number
- K241849 FDA 510(k)
- FDA Product Code
- IZQ FDA 510(k)
- Models / Variants
- MEDRAD Centargo CT Injection System FDA 510(k)MEDRAD Centargo Day Set FDA 510(k)MEDRAD Centargo Patient Line FDA 510(k)MEDRAD Centargo Replacement Spike FDA 510(k)MEDRAD ISI2 Module (ISI2) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.1650 FDA 510(k)
- Regulation Number
- 870.1650 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
MEDRAD Centargo CT Injection System - MEDRAD Centargo Replacement Spike by Imaxeon Pty Ltd — Class II — FDA_510K — listed in FDA 510(k) — 5 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K241849 | Class II | Active |
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Manufacturer
- Manufacturer
- Imaxeon Pty Ltd
- FDA Applicant
- Imaxeon Pty, Ltd.
Sources (1)
- FDA 510(k) K241849 24 fields · synced Jun 18, 2026