Disposable Sucker System

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

510(k) Number

K801400 ↗

FDA Product Code

DTS

Device Class

Class II

Regulation

21 CFR Part 870.4420

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Disposable Parallel Y Connectors

  Class I

  FDA 510(k) K802541 Active Cleared 16 Jan 1981

• Disposable Stopcock

  Class II

  FDA 510(k) K810532 Active Cleared 23 Apr 1981

• Ridgid Vena Cava Cannulae

  Class II

  FDA 510(k) K802543 Active Cleared 16 Jan 1981

• Coronary Perfusion Connector Plug

  Class II

  FDA 510(k) K801399 Active Cleared 30 Jun 1980

• Surgifresh Surgical Smoke Removal

  Not classified

  FDA 510(k) K870932 Active Cleared 31 Mar 1987

• Cardiotomy Filter

  Class II

  FDA 510(k) K830634 Active Cleared 30 Jun 1983

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