Cleared Traditional

K841597 - GIL-MED PARENTERAL NUTRITION OR MEDICINE

K841597 is the FDA 510(k) clearance for GIL-MED PARENTERAL NUTRITION OR MEDICINE by Gil-Med Industries C/O Kegan & Kegan, Ltd.. It is a Class 2 General Hospital device (product code KPE) cleared through the Traditional 510(k) pathway after a 191-day FDA review.

K841597 · Gil-Med Industries C/O Kegan & Kegan, Ltd. · General Hospital
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Oct 1984
Decision
191d
Days
Class 2
Risk

K841597 is an FDA 510(k) clearance for the GIL-MED PARENTERAL NUTRITION OR MEDICINE. Classified as Container, I.v. (product code KPE), Class II - Special Controls.

Submitted by Gil-Med Industries C/O Kegan & Kegan, Ltd. (Chicago, US). The FDA issued a Cleared decision on October 26, 1984 after a review of 191 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5025 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Gil-Med Industries C/O Kegan & Kegan, Ltd. devices

Submission Details

510(k) Number K841597 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 18, 1984
Decision Date October 26, 1984
Days to Decision 191 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d slower than avg
Panel avg: 129d · This submission: 191d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KPE Container, I.v.
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5025
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 - KPE Container, I.v.

All 39
Devices cleared under the same product code (KPE) and FDA review panel - the closest regulatory comparables to K841597.
BAG DECANTER
K852777 · Advance Medical Designs, Inc. · Aug 1985
BOTTLE DECANTER
K852778 · Advance Medical Designs, Inc. · Aug 1985
NUTRIMIX EMPTY CONTAINER
K844077 · Abbott Laboratories · Feb 1985
CAT 3040
K830193 · Burron Medical Products, Inc. · Mar 1983
TOTAL PARENTERAL NUTRITION SET BAG
K801652 · Cutter Laboratories, Inc. · Aug 1980
LIFE CARE 1000ML.EMP. CONT. W/AT. Y-TRAN
K791774 · Abbott Laboratories · Oct 1979