Cleared Traditional

K962329 - GLOBAL LOSS OF RESISTANCE SYRINGE GLOR 10

K962329 is the FDA 510(k) clearance for GLOBAL LOSS OF RESISTANCE SYRINGE GLOR 10 by Global Medical Prods, Inc.. It is a Class 2 General Hospital device (product code FMF) cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K962329 · Global Medical Prods, Inc. · General Hospital
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Sep 1996
Decision
87d
Days
Class 2
Risk

K962329 is an FDA 510(k) clearance for the GLOBAL LOSS OF RESISTANCE SYRINGE GLOR 10. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by Global Medical Prods, Inc. (Woodbury, US). The FDA issued a Cleared decision on September 12, 1996 after a review of 87 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 Global Medical Prods, Inc. devices

Submission Details

510(k) Number K962329 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 17, 1996
Decision Date September 12, 1996
Days to Decision 87 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 129d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 250
Devices cleared under the same product code (FMF) and FDA review panel - the closest regulatory comparables to K962329.
BECTON DICKINSON SYRINGE
K980987 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jun 1998
TERUMO DISPOSABLE HYPODERMC SYRINGE
K980181 · Terumo Medical Corp. · Apr 1998
B-D E ML PEN
K980755 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Apr 1998
TERUMO RETRACTABLE NEEDLE (RN) SYRINGE
K953940 · Terumo Medical Corp. · May 1996
BECTON DICKINSON SYRINGSE
K954064 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Nov 1995
GENOTROPIN MIXER
K954337 · Pharmacia, Inc. · Nov 1995