Recovery G2 Filter System - Femoral Delivery Kit, Model Rf-310f +1 more model

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: Recovery G2 Filter System - Femoral Delivery Kit, Model Rf-310f FDA 510(k)
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, Model Rf-310f +1 more model by C. R. Bard, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 2 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	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