Cleared Traditional

K943740 - ROLL-A-WAY SHARPS DISPOSAL SYSTEM (RED AND IVORY)

K943740 is an FDA 510(k) clearance for ROLL-A-WAY SHARPS DISPOSAL SYSTEM (RED ..., manufactured by Premium Plastics, Inc.. The device is a Class 2 General Hospital device with product code FMI cleared through the Traditional 510(k) pathway after a 134-day FDA review.

K943740 · Premium Plastics, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1994
Decision
134d
Days
Class 2
Risk

K943740 is an FDA 510(k) clearance for the ROLL-A-WAY SHARPS DISPOSAL SYSTEM (RED AND IVORY). Classified as Needle, Hypodermic, Single Lumen (product code FMI), Class II - Special Controls.

Submitted by Premium Plastics, Inc. (Chicago, US). The FDA issued a Cleared decision on December 14, 1994 after a review of 134 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5570 - 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 Premium Plastics, Inc. devices

FDA 510(k) Submission Details - K943740

510(k) Number K943740 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 02, 1994
Decision Date December 14, 1994
Days to Decision 134 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
5d slower than avg
Panel avg: 129d · This submission: 134d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FMI Device Classification - Class 2, Special Controls

Product Code FMI Needle, Hypodermic, Single Lumen
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5570
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 - FMI Needle, Hypodermic, Single Lumen

All 508
Devices cleared under the same product code (FMI) and FDA review panel - the closest regulatory comparables to K943740.
SECURE SAFETY INSERT
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POINT OF USE SHARPS A GATOR
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CHEMOTHERAPY SHARPS DISPOSAL CONTAINERS
K943722 · Baxter Healthcare Corp · Nov 1994