Cleared Traditional

K831668 - CONTINU-FLO SOLUTION ADMINISTRATION

K831668 is an FDA 510(k) clearance for CONTINU-FLO SOLUTION ADMINISTRATION, manufactured by Travenol Laboratories, S.A.. The device is a Class 2 General Hospital device with product code FPB cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K831668 · Travenol Laboratories, S.A. · General Hospital
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Aug 1983
Decision
85d
Days
Class 2
Risk

K831668 is an FDA 510(k) clearance for the CONTINU-FLO SOLUTION ADMINISTRATION. Classified as Filter, Infusion Line (product code FPB), Class II - Special Controls.

Submitted by Travenol Laboratories, S.A. (Walker, US). The FDA issued a Cleared decision on August 16, 1983 after a review of 85 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Travenol Laboratories, S.A. devices

FDA 510(k) Submission Details - K831668

510(k) Number K831668 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 23, 1983
Decision Date August 16, 1983
Days to Decision 85 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
44d faster than avg
Panel avg: 129d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FPB Device Classification - Class 2, Special Controls

Product Code FPB Filter, Infusion Line
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FPB Filter, Infusion Line

All 72
Devices cleared under the same product code (FPB) and FDA review panel - the closest regulatory comparables to K831668.
IVEX-INT
K833684 · Abbott Laboratories · Dec 1983
MILLIPORE IVEX INT FILTER UNIT
K832952 · Millipore Corp. · Oct 1983
POSIDYNE SOLUTION CONTAINER FILTER
K831882 · Pall Biomedical Products Co. · Sep 1983
TRILEX
K831315 · Tri-Med, Inc. · Aug 1983
IVFLO-HP & IVFIL-HP FILTER
K831350 · Tri-Med, Inc. · Aug 1983
IVFLO-HP & IVFIL-HP
K823690 · Tri-Med, Inc. · Dec 1982