Cleared Traditional

K831488 - DAVRON PROF. SCRUB BRUSH-DRY/STERILE

K831488 is an FDA 510(k) clearance for DAVRON PROF. SCRUB BRUSH-DRY/STERILE, manufactured by Minnetonka, Inc.. The device is a Class 1 General & Plastic Surgery device with product code GEC cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K831488 · Minnetonka, Inc. · General & Plastic Surgery device
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Jun 1983
Decision
29d
Days
Class 1
Risk

K831488 is an FDA 510(k) clearance for the DAVRON PROF. SCRUB BRUSH-DRY/STERILE. Classified as Brush, Scrub, Operating-room (product code GEC), Class I - General Controls.

Submitted by Minnetonka, Inc. (Walker, US). The FDA issued a Cleared decision on June 8, 1983 after a review of 29 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - 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 Minnetonka, Inc. devices

FDA 510(k) Submission Details - K831488

510(k) Number K831488 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 10, 1983
Decision Date June 08, 1983
Days to Decision 29 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
86d faster than avg
Panel avg: 115d · This submission: 29d
Pathway characteristics
Predicate-based equivalence.

GEC Device Classification - Class 1, General Controls

Product Code GEC Brush, Scrub, Operating-room
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
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 - GEC Brush, Scrub, Operating-room

All 24
Devices cleared under the same product code (GEC) and FDA review panel - the closest regulatory comparables to K831488.
PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES
K854232 · American Pharmaseal Div. Ahsc · Dec 1985
SCRUB MATE DRY STERILE SCRUB BRUSH
K844411 · American Sterilizer Co. · Dec 1984
FOAM CARE ONE STEP PREP
K843636 · Ballard Medical Products · Nov 1984
MEDICAL PRODUCTS FOAM DOUBLE SCRUB #450
K831226 · Ballard Medical Products · May 1983
ARRIRM SCRUB BRUSH/SPONGE
K823173 · The Buckeye Cellulose Corp. · Nov 1982
SURGI-SCRUB V
K822865 · Acme United Corp. · Oct 1982