Cleared Traditional

K930780 - ADV400 TOE CPM

K930780 is an FDA 510(k) clearance for ADV400 TOE CPM, manufactured by Advanced Kinetics, Inc.. The device is a Class 1 Physical Medicine device with product code BXB cleared through the Traditional 510(k) pathway after a 366-day FDA review.

K930780 · Advanced Kinetics, Inc. · Physical Medicine device
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Feb 1994
Decision
366d
Days
Class 1
Risk

K930780 is an FDA 510(k) clearance for the ADV400 TOE CPM. Classified as Exerciser, Powered (product code BXB), Class I - General Controls.

Submitted by Advanced Kinetics, Inc. (Concord, US). The FDA issued a Cleared decision on February 17, 1994 after a review of 366 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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 Advanced Kinetics, Inc. devices

FDA 510(k) Submission Details - K930780

510(k) Number K930780 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 16, 1993
Decision Date February 17, 1994
Days to Decision 366 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
251d slower than avg
Panel avg: 115d · This submission: 366d
Pathway characteristics
Predicate-based equivalence.

BXB Device Classification - Class 1, General Controls

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.

Regulatory Peers - BXB Exerciser, Powered

All 39
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