Cleared Traditional

2 GALLON ALTERNATE CARE SHARPS CONTAINER

K973911 · Sage Products, Inc. · General Hospital
Oct 1997
Decision
15d
Days
Class 2
Risk

About This 510(k) Submission

K973911 is an FDA 510(k) clearance for the 2 GALLON ALTERNATE CARE SHARPS CONTAINER, a Needle, Hypodermic, Single Lumen (Class II — Special Controls, product code FMI), submitted by Sage Products, Inc. (Crystal Lake, US). The FDA issued a Cleared decision on October 29, 1997, 15 days after receiving the submission on October 14, 1997. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5570.

Submission Details

510(k) Number K973911 FDA.gov
FDA Decision Cleared SESE
Date Received October 14, 1997
Decision Date October 29, 1997
Days to Decision 15 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

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

Similar Devices — FMI Needle, Hypodermic, Single Lumen

All 684
Pen Needle
K252886 · Hh Global Technology, Inc. · Jan 2026
Pen Injector Needle 32.5
K250700 · Terumo Corporation · Nov 2025
Profoject? Disposable Needle
K252631 · CMT Health PTE., Ltd. · Oct 2025
Intraosseous Infusion Needles
K250724 · Spectrum Vascular · Jul 2025
TSK SELECT? Needle
K250284 · Tsk Laboratory, Japan · Jul 2025
K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB)
K251447 · Terumo Europe N.V. · Jul 2025