Cleared Traditional

K901203 - HYPODERMIC SYRINGE LUER LOK

K901203 is an FDA 510(k) clearance for HYPODERMIC SYRINGE LUER LOK, manufactured by Ware-Medics Glass Works, Inc.. The device is a Class 2 General Hospital device with product code FMF cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K901203 · Ware-Medics Glass Works, Inc. · General Hospital
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Jun 1990
Decision
84d
Days
Class 2
Risk

K901203 is an FDA 510(k) clearance for the HYPODERMIC SYRINGE LUER LOK. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by Ware-Medics Glass Works, Inc. (Pearl River, US). The FDA issued a Cleared decision on June 6, 1990 after a review of 84 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5860 - 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 Ware-Medics Glass Works, Inc. devices

FDA 510(k) Submission Details - K901203

510(k) Number K901203 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 14, 1990
Decision Date June 06, 1990
Days to Decision 84 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
45d faster than avg
Panel avg: 129d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FMF Device Classification - Class 2, Special Controls

Product Code FMF Syringe, Piston
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5860
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 - FMF Syringe, Piston

All 539
Devices cleared under the same product code (FMF) and FDA review panel - the closest regulatory comparables to K901203.
B-D(TM) MICROFINE(TM) IV PEN INJECTOR CAT. #328204
K912330 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Oct 1991
JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR
K902157 · Johnson & Johnson Medical, Inc. · Nov 1990
DISPOSABLE CORONARY CONTROL SYRINGE
K902346 · Advance Medical Designs, Inc. · Jun 1990
AUTOPEN
K895890 · Ulster Scientific, Inc. · Feb 1990
INTOPO
K894206 · Acacia, Inc. · Oct 1989
30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES
K894801 · Advance Medical Designs, Inc. · Sep 1989