Cleared Traditional

K844290 - L100D PATIENT CIRCUIT DUAL LINE

K844290 is an FDA 510(k) clearance for L100D PATIENT CIRCUIT DUAL LINE, manufactured by Life Products, Inc.. The device is a Class 1 Anesthesiology device with product code BZO cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K844290 · Life Products, Inc. · Anesthesiology device
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Jan 1985
Decision
66d
Days
Class 1
Risk

K844290 is an FDA 510(k) clearance for the L100D PATIENT CIRCUIT DUAL LINE. Classified as Set, Tubing And Support, Ventilator (w Harness) (product code BZO), Class I - General Controls.

Submitted by Life Products, Inc. (Boulder, US). The FDA issued a Cleared decision on January 10, 1985 after a review of 66 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5975 - 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 Life Products, Inc. devices

FDA 510(k) Submission Details - K844290

510(k) Number K844290 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 05, 1984
Decision Date January 10, 1985
Days to Decision 66 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
74d faster than avg
Panel avg: 140d · This submission: 66d
Pathway characteristics
Predicate-based equivalence.

BZO Device Classification - Class 1, General Controls

Product Code BZO Set, Tubing And Support, Ventilator (w Harness)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5975
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 - BZO Set, Tubing And Support, Ventilator (w Harness)

All 53
Devices cleared under the same product code (BZO) and FDA review panel - the closest regulatory comparables to K844290.
DISPOSABLE VENTILATOR CIRCUITS
K860879 · Dhd Medical Products Div. Diemolding Corp. · Mar 1986
VENTILATOR CIRCUITS (VARIOUS TYPES)
K860880 · Dhd Medical Products Div. Diemolding Corp. · Mar 1986
SAF T FLO VENTILATOR TUBING
K850703 · Bivona Medical Technologies · Mar 1985
PATIENT BREATHING CIRCUIT
K843036 · Infrasonics Corp. · Aug 1984
PATIENT TUBING HYTREL SIEMENS-ELEMA
K841657 · Siemens Elema AB · May 1984
MASS SPECTROMETER INTERFACE
K841722 · Dryden Corp. · May 1984