Cleared Traditional

K874430 - NEEDLE CONTAINER

K874430 is an FDA 510(k) clearance for NEEDLE CONTAINER, manufactured by American Medical Technology, Inc.. The device is a Class 2 General Hospital device with product code FMI cleared through the Traditional 510(k) pathway after a 68-day FDA review.

K874430 · American Medical Technology, Inc. · General Hospital
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Jan 1988
Decision
68d
Days
Class 2
Risk

K874430 is an FDA 510(k) clearance for the NEEDLE CONTAINER. Classified as Needle, Hypodermic, Single Lumen (product code FMI), Class II - Special Controls.

Submitted by American Medical Technology, Inc. (Brooklyn, US). The FDA issued a Cleared decision on January 4, 1988 after a review of 68 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K874430

510(k) Number K874430 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 28, 1987
Decision Date January 04, 1988
Days to Decision 68 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 129d · This submission: 68d
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 695
Devices cleared under the same product code (FMI) and FDA review panel - the closest regulatory comparables to K874430.
BLOOD COLLECTING NEEDLE AND HOLDERS
K880892 · Abco Dealers, Inc. · Apr 1988
ASD-BIO ANTI-STICK DEVICE
K874602 · Biosurge, Inc. · Feb 1988
HYPODERMIC NEEDLES, SINGLE LUMEN
K874414 · Harbor Medical Devices, Inc. · Jan 1988
LAKE IRRIGATION TRAY
K873991 · Lake Medical Products, Inc. · Dec 1987
CHEMO-PORT NON-CORING NEEDLES
K873165 · Hdc Corp. · Dec 1987
ACU-MICRO-NEEDLE
K874024 · Acuderm, Inc. · Nov 1987
K874430 · NEEDLE CONTAINER
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