Cleared Traditional

K850274 - SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT (FDA 510(k) Clearance)

Class I Physical Medicine device.

K850274 · Sutter Biomedical, Inc. · Physical Medicine device
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Apr 1985
Decision
92d
Days
Class 1
Risk

K850274 is an FDA 510(k) clearance for the SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT. Classified as Exerciser, Powered (product code BXB), Class I - General Controls.

Submitted by Sutter Biomedical, Inc. (San Diego, US). The FDA issued a Cleared decision on April 25, 1985 after a review of 92 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5380 - the FDA physical medicine 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 Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Sutter Biomedical, Inc. devices

Submission Details

510(k) Number K850274 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 23, 1985
Decision Date April 25, 1985
Days to Decision 92 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
23d faster than avg
Panel avg: 115d · This submission: 92d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code BXB Exerciser, Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5380
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.