Cleared Traditional

K833452 - OHIO GMS ABSORBER (FDA 510(k) Clearance)

Class I Anesthesiology device.

K833452 · Airco/Ohio Medical Products · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1983
Decision
67d
Days
Class 1
Risk

K833452 is an FDA 510(k) clearance for the OHIO GMS ABSORBER. Classified as Absorber, Carbon-dioxide (product code BSF), Class I - General Controls.

Submitted by Airco/Ohio Medical Products (Mchenry, US). The FDA issued a Cleared decision on November 29, 1983 after a review of 67 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 Airco/Ohio Medical Products devices

Submission Details

510(k) Number K833452 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 1983
Decision Date November 29, 1983
Days to Decision 67 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
72d faster than avg
Panel avg: 139d · This submission: 67d
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.