Cleared Traditional

CRYO MASSAGE CUP (K843203) - FDA 510(k) Clearance

K843203 · Cryo Therapy · Physical Medicine device
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Nov 1984
Decision
92d
Days
-
Risk

K843203 is an FDA 510(k) clearance for the CRYO MASSAGE CUP.

Submitted by Cryo Therapy (Monticelo, US). The FDA issued a Cleared decision on November 14, 1984 after a review of 92 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel. 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.

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Submission Details

510(k) Number K843203 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 14, 1984
Decision Date November 14, 1984
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 -
Device Class -