Cleared Traditional

K914034 - INFUCARE SYRINGE PUMP TUBING SET

K914034 is an FDA 510(k) clearance for INFUCARE SYRINGE PUMP TUBING SET, manufactured by Infucare Products, Inc.. The device is a Class 2 General Hospital device with product code FRN cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K914034 · Infucare Products, Inc. · General Hospital
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Oct 1991
Decision
50d
Days
Class 2
Risk

K914034 is an FDA 510(k) clearance for the INFUCARE SYRINGE PUMP TUBING SET. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Infucare Products, Inc. (Tarpon Springs, US). The FDA issued a Cleared decision on October 30, 1991 after a review of 50 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5725 - 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 Infucare Products, Inc. devices

FDA 510(k) Submission Details - K914034

510(k) Number K914034 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 10, 1991
Decision Date October 30, 1991
Days to Decision 50 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 129d · This submission: 50d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FRN Device Classification - Class 2, Special Controls

Product Code FRN Pump, Infusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5725
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 - FRN Pump, Infusion

All 615
Devices cleared under the same product code (FRN) and FDA review panel - the closest regulatory comparables to K914034.
PANCRETEC I.V. MODEL 5000 INFUS DEVICE, MODIFIED
K913718 · Abbott Laboratories · Oct 1991
PANCRETEC I.V. MODEL 5500 INFUSER
K913719 · Abbott Laboratories · Oct 1991
PANCRETEC PROVIDER ONE INFUSION SYSTEM, MODIFIED
K913720 · Abbott Laboratories · Oct 1991
FLO-GARD(R) 6200, 6300 & 8000
K913895 · Baxter Healthcare Corp · Oct 1991
AVI MODEL 840D DUAL CHANNEL INFUSION PUMP
K912589 · 3M Avi, Inc. · Oct 1991
AVI MODEL 400D INFUSION PUMP
K912590 · 3M Avi, Inc. · Oct 1991