Cleared Traditional

K883009 - NON-CORING NEEDLES

K883009 is an FDA 510(k) clearance for NON-CORING NEEDLES, manufactured by Quinton, Inc.. The device is a Class 2 General Hospital device with product code FMI cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K883009 · Quinton, Inc. · General Hospital
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Oct 1988
Decision
77d
Days
Class 2
Risk

K883009 is an FDA 510(k) clearance for the NON-CORING NEEDLES. Classified as Needle, Hypodermic, Single Lumen (product code FMI), Class II - Special Controls.

Submitted by Quinton, Inc. (Seattle, US). The FDA issued a Cleared decision on October 4, 1988 after a review of 77 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 Quinton, Inc. devices

FDA 510(k) Submission Details - K883009

510(k) Number K883009 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 1988
Decision Date October 04, 1988
Days to Decision 77 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
52d faster than avg
Panel avg: 129d · This submission: 77d
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 486
Devices cleared under the same product code (FMI) and FDA review panel - the closest regulatory comparables to K883009.
SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE
K890926 · Meadox Surgimed, Inc. · Jun 1989
STRAIGHT AND RIGHT ANGLE NON-CORING NEEDLES
K884211 · Marquette Medical, Inc. · Oct 1988
WINGED NON-CORING NEEDLE SET
K884212 · Marquette Medical, Inc. · Oct 1988
VIGGO VASCUPORT NEEDLE
K881758 · Ohmeda Medical · Jun 1988
BLOOD COLLECTING NEEDLE AND HOLDERS
K880892 · Abco Dealers, Inc. · Apr 1988
CHEMO-PORT NON-CORING NEEDLES
K873165 · Hdc Corp. · Dec 1987