Cleared Traditional

K843690 - ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE

K843690 is an FDA 510(k) clearance for ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE, manufactured by Popper & Sons, Inc.. The device is a Class 1 General & Plastic Surgery device with product code GDM cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K843690 · Popper & Sons, Inc. · General & Plastic Surgery device
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Oct 1984
Decision
36d
Days
Class 1
Risk

K843690 is an FDA 510(k) clearance for the ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE. Classified as Needle, Aspiration And Injection, Reusable (product code GDM), Class I - General Controls.

Submitted by Popper & Sons, Inc. (New Hyde Park, US). The FDA issued a Cleared decision on October 25, 1984 after a review of 36 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - the FDA general and plastic surgery 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 Popper & Sons, Inc. devices

FDA 510(k) Submission Details - K843690

510(k) Number K843690 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 19, 1984
Decision Date October 25, 1984
Days to Decision 36 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 115d · This submission: 36d
Pathway characteristics
Predicate-based equivalence.

GDM Device Classification - Class 1, General Controls

Product Code GDM Needle, Aspiration And Injection, Reusable
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - GDM Needle, Aspiration And Injection, Reusable

All 25
Devices cleared under the same product code (GDM) and FDA review panel - the closest regulatory comparables to K843690.
ANGIOMED VAC-U-CUT BIOPSY NEEDLE
K862805 · Angiomed U.S., Inc. · Sep 1986
CIVCO/KEMPF ASPIRATION/BIOPSY/DIALYSIS NEEDLE
K862481 · CIVCO Medical Instruments Co., Inc. · Jul 1986
MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDL
K854420 · Meadox Surgimed, Inc. · Nov 1985
FRANZEN NEEDLE GUIDE
K830235 · Precision Dynamics Corp. · Feb 1983
ISLAM BONE MARROW BIOPSY NEEDLE
K820339 · Downs Surgical , Ltd. · Feb 1982
FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE
K800406 · A.D.T. Lab Industries · Mar 1980