Cleared Traditional

K942076 - TONGUE SCRAPER

K942076 is an FDA 510(k) clearance for TONGUE SCRAPER, manufactured by Maharishi Ayur-Ved. The device is a Class 1 Dental device with product code LCN cleared through the Traditional 510(k) pathway after a 116-day FDA review.

K942076 · Maharishi Ayur-Ved · Dental device
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Aug 1994
Decision
116d
Days
Class 1
Risk

K942076 is an FDA 510(k) clearance for the TONGUE SCRAPER. Classified as Scraper, Tongue (product code LCN), Class I - General Controls.

Submitted by Maharishi Ayur-Ved (Lancaster, US). The FDA issued a Cleared decision on August 23, 1994 after a review of 116 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Maharishi Ayur-Ved devices

FDA 510(k) Submission Details - K942076

510(k) Number K942076 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 29, 1994
Decision Date August 23, 1994
Days to Decision 116 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
11d faster than avg
Panel avg: 127d · This submission: 116d
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 K942076.
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