Portex Hypodermic Needle- Pro Edge Safety Device, 18GX1, 401810, 19GX1, 401910, 20GX1, 402010, 21GX1402110

by Smiths Medical Asd, Inc.

510(k) K063450

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 22 Oct 2026

Documents

510(k) K063450↗

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Abbreviated	NumberK063450	Date25 Jan 2007Cleared	StatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K063450
FDA Product Code: FMI

Device Class: Class II
Regulation: 21 CFR Part 880.5570
Advisory Committee: General Hospital
FDA Decision: SESE Substantially Equivalent

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