Cleared Traditional

K896292 - 1.2 MICRON FILTER WITH IV SET

K896292 is an FDA 510(k) clearance for 1.2 MICRON FILTER WITH IV SET, manufactured by Kendall Mcgaw Laboratories, Inc.. The device is a Class 2 General Hospital device with product code FPB cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K896292 · Kendall Mcgaw Laboratories, Inc. · General Hospital
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Dec 1989
Decision
38d
Days
Class 2
Risk

K896292 is an FDA 510(k) clearance for the 1.2 MICRON FILTER WITH IV SET. Classified as Filter, Infusion Line (product code FPB), Class II - Special Controls.

Submitted by Kendall Mcgaw Laboratories, Inc. (Santa Ana, US). The FDA issued a Cleared decision on December 8, 1989 after a review of 38 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 Kendall Mcgaw Laboratories, Inc. devices

FDA 510(k) Submission Details - K896292

510(k) Number K896292 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 31, 1989
Decision Date December 08, 1989
Days to Decision 38 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
91d faster than avg
Panel avg: 129d · This submission: 38d
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 61
Devices cleared under the same product code (FPB) and FDA review panel - the closest regulatory comparables to K896292.
IVEX-HP96 EXTENDED LIFE FILTER SET
K920736 · Abbott Laboratories · Apr 1993
IVEX-TPN EXTENSION FILTER SET
K913308 · Abbott Laboratories · Jan 1992
PALL 3N1 FILTER
K905794 · Pall Biomedical Products Co. · Jun 1991
LABELING CHANGE FOR CUTTER PUREFLO PLUS IV FILTER
K880605 · Miles Laboratories, Inc. · May 1988
CHURCHILL 0.22 MICRON LIQUID FILTER SETS
K880025 · Churchill Corp. · Apr 1988
CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETS
K880026 · Churchill Corp. · Apr 1988