Cleared Traditional

K962886 - ANESTHESIA CONDUCTION NEEDLE

K962886 is an FDA 510(k) clearance for ANESTHESIA CONDUCTION NEEDLE, manufactured by Ispg, Inc.. The device is a Class 2 Anesthesiology device with product code BSP cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K962886 · Ispg, Inc. · Anesthesiology device
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Oct 1996
Decision
77d
Days
Class 2
Risk

K962886 is an FDA 510(k) clearance for the ANESTHESIA CONDUCTION NEEDLE. Classified as Needle, Conduction, Anesthetic (w/wo Introducer) (product code BSP), Class II - Special Controls.

Submitted by Ispg, Inc. (New Milford, US). The FDA issued a Cleared decision on October 9, 1996 after a review of 77 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 Ispg, Inc. devices

FDA 510(k) Submission Details - K962886

510(k) Number K962886 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 24, 1996
Decision Date October 09, 1996
Days to Decision 77 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
63d faster than avg
Panel avg: 140d · This submission: 77d
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 92
Devices cleared under the same product code (BSP) and FDA review panel - the closest regulatory comparables to K962886.
DOUBLE-HOLE PENCILE-POINT SPINAL NEEDLE (DHPP SPINAL NEEDLE)
K951928 · Csen , Ltd. · May 1997
SPINAL NEEDLES
K961151 · Hakko Shoji Co., Ltd. · Mar 1997
TUOHY EPIDURAL NEEDLES
K961152 · Hakko Shoji Co., Ltd. · Mar 1997
GLOBAL MEDICAL COMBINED SPINAL EPIDURAL KIT (GMA 1827 AND GMA 1725)
K961444 · Global Medical Products, Ltd. · Aug 1996
CLEAR HUB SPINAL NEEDLE, 18, 20, 22, 25 GA.
K951949 · Baxter Healthcare Corp · Aug 1995
MONOJECT WHITACRE POINT SPINAL NEEDLE (27G X 3 1/2)
K951312 · Sherwood Medical Co. · May 1995