Scimed Transend Ex Steerable Guide Wire and Accessories

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K934122 ↗

FDA Product Code

DQX

Device Class

Class II

Regulation

21 CFR Part 870.1330

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Scimed(R) Venture(Tm) II Infusion Catheter

  Class II

  FDA 510(k) K945904 Active Cleared 19 May 1995

• Scimed Transent Ex Steerable Guide Wire and Accessories

  Class II

  FDA 510(k) K944677 Active Cleared 8 Feb 1995

• Scimed(R) Courier Guide Catheter

  Class II

  FDA 510(k) K946272 Active Cleared 17 Apr 1995

• Scimed Strike Steerable Guide Wire

  Class II

  FDA 510(k) K934359 Active Cleared 7 Oct 1993

• Scimed Maverick

  Class II

  FDA 510(k) K934793 Active Cleared 5 Jan 1994

• Scimed Transend Steerable Guide Wire and Accessories

  Class II

  FDA 510(k) K941710 Active Cleared 1 Sep 1994

See all devices from Scimed Peripheral Interventions →