Cleared Traditional

K801776 - COLD PACK #589 (FDA 510(k) Clearance)

Class I Physical Medicine device.

K801776 · Sunbeam Corp. · Physical Medicine device
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Aug 1980
Decision
10d
Days
Class 1
Risk

K801776 is an FDA 510(k) clearance for the COLD PACK #589. Classified as Pack, Hot Or Cold, Reusable (product code IME), Class I - General Controls.

Submitted by Sunbeam Corp. (Mchenry, US). The FDA issued a Cleared decision on August 7, 1980 after a review of 10 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5700 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Sunbeam Corp. devices

Submission Details

510(k) Number K801776 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 1980
Decision Date August 07, 1980
Days to Decision 10 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
105d faster than avg
Panel avg: 115d · This submission: 10d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code IME Pack, Hot Or Cold, Reusable
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5700
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.