Cleared Traditional

K880553 - ELECTRONIC EPILATOR

K880553 is an FDA 510(k) clearance for ELECTRONIC EPILATOR, manufactured by Clareblend, Inc.. The device is a Class 1 General & Plastic Surgery device with product code KCW cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K880553 · Clareblend, Inc. · General & Plastic Surgery device
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Feb 1988
Decision
20d
Days
Class 1
Risk

K880553 is an FDA 510(k) clearance for the ELECTRONIC EPILATOR. Classified as Epilator, High Frequency, Needle-type (product code KCW), Class I - General Controls.

Submitted by Clareblend, Inc. (Sylmar, US). The FDA issued a Cleared decision on February 29, 1988 after a review of 20 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.5350 - the FDA general and plastic surgery 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 Clareblend, Inc. devices

FDA 510(k) Submission Details - K880553

510(k) Number K880553 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 09, 1988
Decision Date February 29, 1988
Days to Decision 20 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 115d · This submission: 20d
Pathway characteristics
Predicate-based equivalence.

KCW Device Classification - Class 1, General Controls

Product Code KCW Epilator, High Frequency, Needle-type
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.5350
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.