Outback Ltd Re-Entry Catheter, Model: OTB42120

by Cordis Corp., A Johnson & Johnson Co.

510(k) K083814

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 10 Oct 2026

Documents

510(k) K083814↗

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 10 Oct 2026. What this means

Regulatory status

as of registry sync 10 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK083814	Date13 Jan 2009Cleared	StatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 10 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K083814
FDA Product Code: PDU

Device Class: Class II
Regulation: 21 CFR Part 870.1250
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

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