Cleared Traditional

K873476 - MINI-MOTOR HAND ENGINE & ACCESS. DERMAB...

K873476 is the FDA 510(k) clearance for MINI-MOTOR HAND ENGINE & ACCESS. DERMAB... by Mcghan Medical Corp.. It is a Class 1 General & Plastic Surgery device (product code GEY) cleared through the Traditional 510(k) pathway after a 11-day FDA review.

K873476 · Mcghan Medical Corp. · General & Plastic Surgery device
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Sep 1987
Decision
11d
Days
Class 1
Risk

K873476 is an FDA 510(k) clearance for the MINI-MOTOR HAND ENGINE & ACCESS. DERMABRASION BURS. Classified as Motor, Surgical Instrument, Ac-powered (product code GEY), Class I - General Controls.

Submitted by Mcghan Medical Corp. (Santa Barbara, US). The FDA issued a Cleared decision on September 11, 1987 after a review of 11 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4820 - 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 Mcghan Medical Corp. devices

Submission Details

510(k) Number K873476 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 1987
Decision Date September 11, 1987
Days to Decision 11 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
104d faster than avg
Panel avg: 115d · This submission: 11d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GEY Motor, Surgical Instrument, Ac-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4820
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 - GEY Motor, Surgical Instrument, Ac-powered

All 18
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