Cleared Traditional

K830165 - BEAR JET 150 VENTILATOR

K830165 is an FDA 510(k) clearance for BEAR JET 150 VENTILATOR, manufactured by Bear Medical Systems, Inc.. The device is a Class 2 General Hospital device with product code FLI cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K830165 · Bear Medical Systems, Inc. · General Hospital
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Apr 1983
Decision
84d
Days
Class 2
Risk

K830165 is an FDA 510(k) clearance for the BEAR JET 150 VENTILATOR. Classified as Cabinet, Ethylene-oxide Gas Aerator (product code FLI), Class II - Special Controls.

Submitted by Bear Medical Systems, Inc. (Walker, US). The FDA issued a Cleared decision on April 12, 1983 after a review of 84 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6100 - the FDA general hospital 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 Bear Medical Systems, Inc. devices

FDA 510(k) Submission Details - K830165

510(k) Number K830165 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 18, 1983
Decision Date April 12, 1983
Days to Decision 84 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
45d faster than avg
Panel avg: 129d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FLI Device Classification - Class 2, Special Controls

Product Code FLI Cabinet, Ethylene-oxide Gas Aerator
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6100
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 General Hospital devices follow this clearance model.