Cleared Traditional

K801839 - DISPOSABLE HYPODERMIC NEEDLES

K801839 is an FDA 510(k) clearance for DISPOSABLE HYPODERMIC NEEDLES, manufactured by Martin'S Maine Exchange. The device is a Class 2 General Hospital device with product code FMI cleared through the Traditional 510(k) pathway after a 46-day FDA review.

K801839 · Martin'S Maine Exchange · General Hospital
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Sep 1980
Decision
46d
Days
Class 2
Risk

K801839 is an FDA 510(k) clearance for the DISPOSABLE HYPODERMIC NEEDLES. Classified as Needle, Hypodermic, Single Lumen (product code FMI), Class II - Special Controls.

Submitted by Martin'S Maine Exchange (Mchenry, US). The FDA issued a Cleared decision on September 16, 1980 after a review of 46 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.

View all Martin'S Maine Exchange devices

FDA 510(k) Submission Details - K801839

510(k) Number K801839 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 01, 1980
Decision Date September 16, 1980
Days to Decision 46 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
83d faster than avg
Panel avg: 129d · This submission: 46d
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 495
Devices cleared under the same product code (FMI) and FDA review panel - the closest regulatory comparables to K801839.
HYPOSERMIC NEEDLES
K813545 · Optical Micro Systems, Inc. · Jan 1982
MEDISYSTEMS NEEDLES & SYRINGES
K812910 · Medisystems Corp. · Nov 1981
VISITEC NEEDLE RANGE (GENERAL HOSPITAL)
K811966 · Visitec Co. · Jul 1981
DOUBLE ENDED FILTERED TRANSFER NEEDLE
K801107 · Burron Medical Products, Inc. · May 1980
DOUBLE ENDED VENTED TRANSFER DEVICE
K801108 · Burron Medical Products, Inc. · May 1980
AMIPAQUE MYELOGRAM TRAY
K791156 · Pharmaseal Div., Baxter Healthcare Corp. · Jul 1979