Cleared Traditional

K920590 - OHMEDA MODEL 5250 RGM MONITOR

K920590 is an FDA 510(k) clearance for OHMEDA MODEL 5250 RGM MONITOR, manufactured by Ohmeda Medical. The device is a Class 2 Anesthesiology device with product code CCK cleared through the Traditional 510(k) pathway after a 203-day FDA review.

K920590 · Ohmeda Medical · Anesthesiology device
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Aug 1992
Decision
203d
Days
Class 2
Risk

K920590 is an FDA 510(k) clearance for the OHMEDA MODEL 5250 RGM MONITOR. Classified as Analyzer, Gas, Carbon-dioxide, Gaseous-phase (product code CCK), Class II - Special Controls.

Submitted by Ohmeda Medical (Louisville, US). The FDA issued a Cleared decision on August 31, 1992 after a review of 203 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1400 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Ohmeda Medical devices

FDA 510(k) Submission Details - K920590

510(k) Number K920590 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 10, 1992
Decision Date August 31, 1992
Days to Decision 203 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
63d slower than avg
Panel avg: 140d · This submission: 203d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CCK Device Classification - Class 2, Special Controls

Product Code CCK Analyzer, Gas, Carbon-dioxide, Gaseous-phase
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1400
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 - CCK Analyzer, Gas, Carbon-dioxide, Gaseous-phase

All 231
Devices cleared under the same product code (CCK) and FDA review panel - the closest regulatory comparables to K920590.
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K915228 · Hospitak, Inc. · Feb 1992
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K911193 · Ohmeda Medical · Aug 1991