Cleared Traditional

K800650 - MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM

K800650 is the FDA 510(k) clearance for MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM by Hospal Medical Corp.. It is a Class 2 Anesthesiology device (product code CBK) cleared through the Traditional 510(k) pathway after a 9-day FDA review.

K800650 · Hospal Medical Corp. · Anesthesiology device
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Apr 1980
Decision
9d
Days
Class 2
Risk

K800650 is an FDA 510(k) clearance for the MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM. Classified as Ventilator, Continuous, Facility Use (product code CBK), Class II - Special Controls.

Submitted by Hospal Medical Corp. (Mchenry, US). The FDA issued a Cleared decision on April 2, 1980 after a review of 9 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5895 - 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 Hospal Medical Corp. devices

Submission Details

510(k) Number K800650 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 24, 1980
Decision Date April 02, 1980
Days to Decision 9 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
131d faster than avg
Panel avg: 140d · This submission: 9d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CBK Ventilator, Continuous, Facility Use
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5895
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - CBK Ventilator, Continuous, Facility Use

All 196
Devices cleared under the same product code (CBK) and FDA review panel - the closest regulatory comparables to K800650.
DRAGER AV2 ANESTHESIA VENTILATOR
K802168 · Draeger Medical, Inc. · Dec 1980
INFANT VENTILATOR, (RESPIRATOR) PLAN B
K802583 · Healthdyne, Inc. · Dec 1980
BABYBIRD 2 VENTILATOR
K802087 · Bird Products Corp. · Oct 1980
SIEMENS-ELEMA AB MANUAL VENTILATION
K800114 · Siemens Elema AB · Mar 1980
VENTILATOR, INFANT MODEL 100
K781926 · Healthdyne, Inc. · Dec 1978
CRITICAL CARE VENTILATOR 2
K772065 · Ohio Medical Products · Nov 1977