Blue Line(R) Pdt(Tm) Portex Directional Tube

by Smiths Industries Medical Systems, Inc.

510(k) K931735

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) K931735↗

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 · Traditional	NumberK931735	Date18 May 1993Cleared	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Withdrawn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: K931735
FDA Product Code: BTR

Device Class: Class II
Regulation: 21 CFR Part 868.5730
Advisory Committee: Anesthesiology
FDA Decision: SESE Substantially Equivalent

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