Stockert-Shiley Caps Venous Occlusion Clamp

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K864890 ↗

FDA Product Code

KRI

Device Class

Class I

Regulation

21 CFR Part 870.4200

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Basic Heater-Cooler Unit, 115/100V 16-02-20

  Class II

  FDA 510(k) K883330 Active Cleared 26 Sep 1988

• Schneider-Shiley Y-Connector with Rotator

  Class II

  FDA 510(k) K862464 Active Cleared 28 Aug 1986

• Expanded Use for Shiley 3l Cardiotomy Reservoir

  Class II

  FDA 510(k) K872721 Active Cleared 23 Sep 1987

• Shiley Venous Reservoir

  Class II

  FDA 510(k) K854841 Active Cleared 10 Feb 1986

• Arterial Embolectomy Catheter

  Class II

  FDA 510(k) K840198 Active Cleared 3 Aug 1984

• Shiley Femoral Arterial Cannula

  Class II

  FDA 510(k) K881072 Active Cleared 31 May 1988

See all devices from Shiley, Inc. →