Cleared Traditional

K760076 - ABSORBER, ANESTHESIA CIRCLE SYS, CO2 (FDA 510(k) Clearance)

Class I Anesthesiology device.

K760076 · Fraser Sweatman, Inc. · Anesthesiology device
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Jul 1976
Decision
28d
Days
Class 1
Risk

K760076 is an FDA 510(k) clearance for the ABSORBER, ANESTHESIA CIRCLE SYS, CO2. Classified as Absorber, Carbon-dioxide (product code BSF), Class I - General Controls.

Submitted by Fraser Sweatman, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 16, 1976 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5310 - 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 Fraser Sweatman, Inc. devices

Submission Details

510(k) Number K760076 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 18, 1976
Decision Date July 16, 1976
Days to Decision 28 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
111d faster than avg
Panel avg: 139d · This submission: 28d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code BSF Absorber, Carbon-dioxide
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5310
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.