Cleared Traditional

K802270 - PROTECTIVE BAR FOR THE MA-1VENTILATOR

K802270 is the FDA 510(k) clearance for PROTECTIVE BAR FOR THE MA-1VENTILATOR by Eastern Anesthesia, Inc.. It is a Class 2 Anesthesiology device (product code CBK) cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K802270 · Eastern Anesthesia, Inc. · Anesthesiology device
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Oct 1980
Decision
16d
Days
Class 2
Risk

K802270 is an FDA 510(k) clearance for the PROTECTIVE BAR FOR THE MA-1VENTILATOR. Classified as Ventilator, Continuous, Facility Use (product code CBK), Class II - Special Controls.

Submitted by Eastern Anesthesia, Inc. (Walker, US). The FDA issued a Cleared decision on October 3, 1980 after a review of 16 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 Eastern Anesthesia, Inc. devices

Submission Details

510(k) Number K802270 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 17, 1980
Decision Date October 03, 1980
Days to Decision 16 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
124d faster than avg
Panel avg: 140d · This submission: 16d
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.