Cleared Traditional

K945485 - ABG NEEDLE PROTECTION

K945485 is an FDA 510(k) clearance for ABG NEEDLE PROTECTION, manufactured by Devon Industries, Inc.. The device is a Class 1 Anesthesiology device with product code CBT cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K945485 · Devon Industries, Inc. · Anesthesiology device
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Nov 1994
Decision
21d
Days
Class 1
Risk

K945485 is an FDA 510(k) clearance for the ABG NEEDLE PROTECTION. Classified as Arterial Blood Sampling Kit (product code CBT), Class I - General Controls.

Submitted by Devon Industries, Inc. (Chatsworth, US). The FDA issued a Cleared decision on November 29, 1994 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1100 - 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 Devon Industries, Inc. devices

FDA 510(k) Submission Details - K945485

510(k) Number K945485 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 08, 1994
Decision Date November 29, 1994
Days to Decision 21 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
119d faster than avg
Panel avg: 140d · This submission: 21d
Pathway characteristics
Predicate-based equivalence.

CBT Device Classification - Class 1, General Controls

Product Code CBT Arterial Blood Sampling Kit
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.1100
Definition This Product Code Has Been Established In Accordance With The May 20, 1997, Guidance Entitled, Convenience Kits Interim Regulatory Guidance, Found At Www.fda.gov/cdrh/ode/convkit.html. This Type Of Convenience Kit, As Listed In The Guidance Above, Is Under Enforcement Discretion, And Does Not Require A Premarket Notification (510(k)) To Market If It Meets All Criteria In The Guidance.
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 - CBT Arterial Blood Sampling Kit

All 34
Devices cleared under the same product code (CBT) and FDA review panel - the closest regulatory comparables to K945485.
ABC IN-LINE BLOOD SAMPLING KIT
K955663 · Utah Medical Products, Inc. · Mar 1997
ABG POINT LOK NEEDLE PROTECTION DEVICE
K954015 · Devon Industries, Inc. · Nov 1995
ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM
K945719 · Sherwood Medical Co. · Mar 1995
ASPIR-PULSE(TM) SAF-T-VENT
K940575 · Sherwood Medical Co. · Mar 1994
BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560
K930986 · Customed, Inc. · Jul 1993
SHERWOOD MEDICAL ARTERIAL BLOOD GAS KIT I
K925453 · Sherwood Medical Co. · Jul 1993