Cleared Traditional

K935011 - SWIMEX MULTIDEPTH POOL (MODEL 600T)

K935011 is an FDA 510(k) clearance for SWIMEX MULTIDEPTH POOL (MODEL 600T), manufactured by Swimex Systems. The device is a Class 1 Physical Medicine device with product code BXB cleared through the Traditional 510(k) pathway after a 446-day FDA review.

K935011 · Swimex Systems · Physical Medicine device
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Jan 1995
Decision
446d
Days
Class 1
Risk

K935011 is an FDA 510(k) clearance for the SWIMEX MULTIDEPTH POOL (MODEL 600T). Classified as Exerciser, Powered (product code BXB), Class I - General Controls.

Submitted by Swimex Systems (Warren, US). The FDA issued a Cleared decision on January 9, 1995 after a review of 446 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Physical Medicine submissions.

View all Swimex Systems devices

FDA 510(k) Submission Details - K935011

510(k) Number K935011 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 20, 1993
Decision Date January 09, 1995
Days to Decision 446 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
331d slower than avg
Panel avg: 115d · This submission: 446d
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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