Cleared Traditional

K955656 - NORTH STATE PLASTICS AEROSOL TEE

K955656 is the FDA 510(k) clearance for NORTH STATE PLASTICS AEROSOL TEE by North State Plastics, Inc.. It is a Class 1 Anesthesiology device (product code BYX) cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K955656 · North State Plastics, Inc. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1996
Decision
85d
Days
Class 1
Risk

K955656 is an FDA 510(k) clearance for the NORTH STATE PLASTICS AEROSOL TEE. Classified as Tubing, Pressure And Accessories (product code BYX), Class I - General Controls.

Submitted by North State Plastics, Inc. (Denver, US). The FDA issued a Cleared decision on March 6, 1996 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5860 - 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 North State Plastics, Inc. devices

Submission Details

510(k) Number K955656 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 12, 1995
Decision Date March 06, 1996
Days to Decision 85 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 140d · This submission: 85d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code BYX Tubing, Pressure And Accessories
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5860
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 - BYX Tubing, Pressure And Accessories

All 8
Devices cleared under the same product code (BYX) and FDA review panel - the closest regulatory comparables to K955656.
OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP
K801190 · Airlife, Inc. · May 1980
CORRUGATED FLEXIBLE POLYETHYLENE & EVA
K791821 · Airlife, Inc. · Sep 1979
TUBING CORRUGATED
K790147 · Airlife, Inc. · Feb 1979
TUBING, E.V.A. FLEXIBLE
K790158 · Airlife, Inc. · Feb 1979
CORRUGATED FLEXIBLE E.V.A. TUBING
K790159 · Airlife, Inc. · Feb 1979
OXYGEN TUBING, W/VINYL AND LATEX TIPS
K790160 · Airlife, Inc. · Feb 1979