Cleared Traditional

K905119 - PLAZLYTE(TM)

K905119 is an FDA 510(k) clearance for PLAZLYTE(TM), manufactured by Abtox, Inc.. The device is a Class 2 General Hospital device with product code FLF cleared through the Traditional 510(k) pathway after a 1499-day FDA review.

K905119 · Abtox, Inc. · General Hospital
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Dec 1994
Decision
1499d
Days
Class 2
Risk

K905119 is an FDA 510(k) clearance for the PLAZLYTE(TM). Classified as Sterilizer, Ethylene-oxide Gas (product code FLF), Class II - Special Controls.

Submitted by Abtox, Inc. (Mundelein, US). The FDA issued a Cleared decision on December 22, 1994 after a review of 1499 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6860 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind General Hospital submissions.

View all Abtox, Inc. devices

FDA 510(k) Submission Details - K905119

510(k) Number K905119 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 1990
Decision Date December 22, 1994
Days to Decision 1499 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
1370d slower than avg
Panel avg: 129d · This submission: 1499d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FLF Device Classification - Class 2, Special Controls

Product Code FLF Sterilizer, Ethylene-oxide Gas
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6860
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 - FLF Sterilizer, Ethylene-oxide Gas

All 16
Devices cleared under the same product code (FLF) and FDA review panel - the closest regulatory comparables to K905119.
TSO3 OZONE STERILIZER, MODEL 125L
K090636 · Tso3, Inc. · Dec 2009
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STERRAD 50 & STERRAD 100S STERILIZERS
K023290 · Advanced Sterilization Products · Apr 2003
STERI-VAC GAS STERILIZER MODEL 8XL
K941748 · 3M Health Care, Ltd. · Dec 1994
THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZER
K931872 · American Sterilizer Co. · Feb 1994
STERRAD 100 STERILIZATION SYSTEM
K915682 · Johnson & Johnson Medical, Inc. · Oct 1993