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RECOVERY G2 FILTER SYSTEM - FEMORAL DELIVERY KIT - Jugular/Subclavain Delivery Kit, Model Rf-320j
FDA 510(k)Class II (US FDA 510(k))
510(k) K073090
Identifiers
- 510(k) Number
- K073090 FDA 510(k)
- FDA Product Code
- DTK FDA 510(k)
- Models / Variants
- Jugular/Subclavain Delivery Kit, Model Rf-320j FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.3375 FDA 510(k)
- Regulation Number
- 870.3375 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
RECOVERY G2 FILTER SYSTEM - FEMORAL DELIVERY KIT - Jugular/Subclavain Delivery Kit, Model Rf-320j by C. R. Bard, Inc. — Class II — FDA_510K — listed in FDA…
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 | K073090 | Class II | Active |
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Manufacturer
- Manufacturer
- C. R. Bard, Inc.
- FDA Applicant
- C.R. Bard, Inc.
Sources (1)
- FDA 510(k) K073090 24 fields · synced Jun 18, 2026