Cleared Traditional

K841455 - REUSEABLE NON-CONDUCTIVE FIXED Y

K841455 is an FDA 510(k) clearance for REUSEABLE NON-CONDUCTIVE FIXED Y, manufactured by Dryden Corp.. The device is a Class 1 Anesthesiology device with product code CAI cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K841455 · Dryden Corp. · Anesthesiology device
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Jun 1984
Decision
63d
Days
Class 1
Risk

K841455 is an FDA 510(k) clearance for the REUSEABLE NON-CONDUCTIVE FIXED Y. Classified as Circuit, Breathing (w Connector, Adaptor, Y Piece) (product code CAI), Class I - General Controls.

Submitted by Dryden Corp. (Mchenry, US). The FDA issued a Cleared decision on June 11, 1984 after a review of 63 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5240 - 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 Dryden Corp. devices

FDA 510(k) Submission Details - K841455

510(k) Number K841455 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 09, 1984
Decision Date June 11, 1984
Days to Decision 63 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 140d · This submission: 63d
Pathway characteristics
Predicate-based equivalence.

CAI Device Classification - Class 1, General Controls

Product Code CAI Circuit, Breathing (w Connector, Adaptor, Y Piece)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5240
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 - CAI Circuit, Breathing (w Connector, Adaptor, Y Piece)

All 116
Devices cleared under the same product code (CAI) and FDA review panel - the closest regulatory comparables to K841455.
AMBU RUBEN CIRCLE ANESTHESIA SYSTEM
K844149 · Ambu, Inc. · Nov 1984
SAMSON 1000 ANESTHESIA CIRCUIT
K842488 · J. H. Emerson Co. · Jul 1984
BABYSET TM & PAC TM -PULMONARY ASSIST
K841264 · Life Design Systems, Inc. · Jun 1984
SCRATCH & SNIFF FOR ANESTHESIA
K840431 · Dryden Corp. · May 1984
CIRCUIT BREATHING
K840740 · Marquest Medical Products, Inc. · Apr 1984
ANESTHESIA VENTILATOR CIRCUIT
K840850 · The Kendal Co. · Mar 1984