Catheter, Cava (Cavafix)

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K760387 ↗

FDA Product Code

DQO

Device Class

Class II

Regulation

21 CFR Part 870.1200

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Extension Sets

  Class I

  FDA 510(k) K760385 Active Cleared 2 Nov 1976

• Catheter, Vein (Venofix)

  Class II

  FDA 510(k) K760388 Active Cleared 2 Nov 1976

• Stoppers

  Class I

  FDA 510(k) K760384 Active Cleared 2 Nov 1976

• Cannula, Iv

  Class I

  FDA 510(k) K760389 Active Cleared 2 Nov 1976

• Connectors

  Class I

  FDA 510(k) K760382 Active Cleared 2 Nov 1976

• Central Veinous Pressure Sets

  Class II

  FDA 510(k) K760386 Active Cleared 2 Nov 1976

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