Cleared Traditional

K850420 - CHURCHILL HABER POINT NEEDLE ADMIN. SET

K850420 is an FDA 510(k) clearance for CHURCHILL HABER POINT NEEDLE ADMIN. SET, manufactured by Churchill Corp.. The device is a Class 2 General Hospital device with product code FMI cleared through the Traditional 510(k) pathway after a 79-day FDA review.

K850420 · Churchill Corp. · General Hospital
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Apr 1985
Decision
79d
Days
Class 2
Risk

K850420 is an FDA 510(k) clearance for the CHURCHILL HABER POINT NEEDLE ADMIN. SET. Classified as Needle, Hypodermic, Single Lumen (product code FMI), Class II - Special Controls.

Submitted by Churchill Corp. (Pineville, US). The FDA issued a Cleared decision on April 24, 1985 after a review of 79 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 Churchill Corp. devices

FDA 510(k) Submission Details - K850420

510(k) Number K850420 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 04, 1985
Decision Date April 24, 1985
Days to Decision 79 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
50d faster than avg
Panel avg: 129d · This submission: 79d
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 473
Devices cleared under the same product code (FMI) and FDA review panel - the closest regulatory comparables to K850420.
HEMED NEEDLE SUPPORT CATALOG NO. HAP-XXXX
K853731 · Gish Biomedical, Inc. · Oct 1985
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JMS NEEDLES & JMS SYRINGES
K845043 · Jms Co., Ltd. · Apr 1985
INFUSET W/HUBER NEEDLE
K844313 · Med Fusion Systems, Inc. · Jan 1985
MONOJECT MENGHINI SOFT TISSUE BIOPSY
K843264 · Sherwood Medical Co. · Dec 1984
AMER. PHARMASEAL CHEMONUCLEOLYSIS TRAY
K842542 · American Pharmaseal Div. Ahsc · Aug 1984