Cleared Traditional

K823692 - SPINAL NEEDLE

K823692 is an FDA 510(k) clearance for SPINAL NEEDLE, manufactured by Ocean Medical Products, Ltd.. The device is a Class 2 Anesthesiology device with product code BSP cleared through the Traditional 510(k) pathway after a 30-day FDA review.

K823692 · Ocean Medical Products, Ltd. · Anesthesiology device
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Jan 1983
Decision
30d
Days
Class 2
Risk

K823692 is an FDA 510(k) clearance for the SPINAL NEEDLE. Classified as Needle, Conduction, Anesthetic (w/wo Introducer) (product code BSP), Class II - Special Controls.

Submitted by Ocean Medical Products, Ltd. (Walker, US). The FDA issued a Cleared decision on January 7, 1983 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5150 - the FDA anesthesiology and respiratory 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 Ocean Medical Products, Ltd. devices

FDA 510(k) Submission Details - K823692

510(k) Number K823692 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 1982
Decision Date January 07, 1983
Days to Decision 30 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
110d faster than avg
Panel avg: 140d · This submission: 30d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BSP Device Classification - Class 2, Special Controls

Product Code BSP Needle, Conduction, Anesthetic (w/wo Introducer)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5150
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - BSP Needle, Conduction, Anesthetic (w/wo Introducer)

All 120
Devices cleared under the same product code (BSP) and FDA review panel - the closest regulatory comparables to K823692.
VYGON SPINAL ANESTHESIA NEEDLE W/INTRODUCER 183
K851478 · Vygon Corp. · May 1985
AIRES TUOHY NEEDLES 17GA. X 4 1/2
K850111 · Aries Medical, Inc. · Jan 1985
EPINEED EPIDURAL NEEDLE
K832233 · Terumo Medical Corp. · Aug 1983
MONOJECT PLASTIC HUB SPINAL NEEDLE
K822630 · Sherwood Medical Co. · Oct 1982
SPINOCAN SPINAL NEEDLE
K820047 · Burron Medical Products, Inc. · Jan 1982
PLEXUFIX BRACHIAL PLEXUS ANESTH. NEEDLE
K813165 · Burron Medical Products, Inc. · Dec 1981