Continu-Flo Solution Administration

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K831668 ↗

FDA Product Code

FPB

Device Class

Class II

Regulation

21 CFR Part 880.5440

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Burette Set with Air Control Lever

  Class II

  FDA 510(k) K780970 Active Cleared 27 Jul 1978

• Sterile Water & Saline in Plastic Btl.

  Class II

  FDA 510(k) K800753 Active Cleared 24 Apr 1980

• Solution Administration Sets

  Class II

  FDA 510(k) K860272 Active Cleared 18 Mar 1986

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• Flo-Gard 8000 Computer Control Infusi

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  FDA 510(k) K834154 Active Cleared 25 Jan 1984

See all devices from Travenol Laboratories, S.A. →

• What is the CONTINU-FLO SOLUTION ADMINISTRATION used for?

  The CONTINU-FLO SOLUTION ADMINISTRATION is designed for administering solutions via intravascular routes in general hospital settings, functioning as a Filter, Infusion Line to support solution delivery during clinical use.

• How is the CONTINU-FLO SOLUTION ADMINISTRATION supplied and what models are available?

  The device is supplied as part of administration sets and includes various models and sizes, such as K831668 and K792538, manufactured by Travenol Laboratories, S.A. for use in general hospital applications.

• Is the CONTINU-FLO SOLUTION ADMINISTRATION sterile and intended for single-use or reuse?

  As a component of infusion administration sets intended for intravascular solution administration, the CONTINU-FLO SOLUTION ADMINISTRATION is designed for single-use to maintain sterility and prevent cross-contamination, consistent with standard infusion set design.