Cleared Traditional

K901408 - THE TONGUE BRUSH

K901408 is an FDA 510(k) clearance for THE TONGUE BRUSH, manufactured by Garry Laboratories, Inc.. The device is a Class 1 Dental device with product code LCN cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K901408 · Garry Laboratories, Inc. · Dental device
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May 1990
Decision
56d
Days
Class 1
Risk

K901408 is an FDA 510(k) clearance for the THE TONGUE BRUSH. Classified as Scraper, Tongue (product code LCN), Class I - General Controls.

Submitted by Garry Laboratories, Inc. (Greenwood, US). The FDA issued a Cleared decision on May 21, 1990 after a review of 56 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6855 - the FDA dental device regulatory 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 Garry Laboratories, Inc. devices

FDA 510(k) Submission Details - K901408

510(k) Number K901408 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 1990
Decision Date May 21, 1990
Days to Decision 56 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 127d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

LCN Device Classification - Class 1, General Controls

Product Code LCN Scraper, Tongue
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6855
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 - LCN Scraper, Tongue

All 19
Devices cleared under the same product code (LCN) and FDA review panel - the closest regulatory comparables to K901408.
OOLITT TONGUE CLEANER, REGULAR LOW RIPPLE/SPECIAL HIGH RIPPLE/LOW RIPPLE DOUBLE/HIGH & LOW RIPPLE/COMFORT EZE
K962941 · Deep Trading Corp. · Oct 1996
TONGUE SCRAPPER
K961574 · U.S. Dentek Corp. · Jun 1996
TONGUE CLEANER
K961660 · Jack Conrey · May 1996
COAT-A-COUNT PCP KIT NUMBER TKPC1
K870875 · Diagnostic Products Corp. · Mar 1987
MEDI-TECH DILATATION CATHETERS
K844292 · Medi-Tech, Inc. · Nov 1984