Cleared Traditional

K082853 - CLINICAL OXYGEN DOSE RECORDER (CODR), MODEL 300-CR (FDA 510(k) Clearance)

Class II Anesthesiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K082853 · Inspired Technologies, Inc. · Anesthesiology device
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Mar 2009
Decision
175d
Days
Class 2
Risk

K082853 is an FDA 510(k) clearance for the CLINICAL OXYGEN DOSE RECORDER (CODR), MODEL 300-CR. Classified as Ventilatory Effort Recorder (product code MNR), Class II - Special Controls.

Submitted by Inspired Technologies, Inc. (Bonita Springs, US). The FDA issued a Cleared decision on March 23, 2009 after a review of 175 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.2375 - 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 Inspired Technologies, Inc. devices

Submission Details

510(k) Number K082853 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2008
Decision Date March 23, 2009
Days to Decision 175 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
36d slower than avg
Panel avg: 139d · This submission: 175d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MNR Ventilatory Effort Recorder
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.2375
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.