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.
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