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PREVIEW FORWARD-LOOKING IVUS CATHETER AND LAPTOP SYSTEM - Pimf Model 87-Pimf
FDA 510(k)Class II (US FDA 510(k))
510(k) K122826
Identifiers
- 510(k) Number
- K122826 FDA 510(k)
- FDA Product Code
- DQY FDA 510(k)
- Models / Variants
- Preview Catheter Model 87000 FDA 510(k)Pimf Model 87-Pimf FDA 510(k)Laptop System FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.1250 FDA 510(k)
- Regulation Number
- 870.1250 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
PREVIEW FORWARD-LOOKING IVUS CATHETER AND LAPTOP SYSTEM - Pimf Model 87-Pimf by Volcano Corporation — Class II — FDA_510K — listed in FDA 510(k) — 4 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 | K122826 | Class II | Active |
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Manufacturer
- Manufacturer
- Volcano Corporation
Sources (1)
- FDA 510(k) K122826 24 fields · synced Jun 19, 2026