510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K882303Substantially Equivalent

H&m Anti-Snoring Device

Hays & Meade, Inc., Albuquerque NM / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K882303 is the FDA 510(k) clearance record for H&M ANTI-SNORING DEVICE, a class II device, cleared for Hays & Meade, Inc. on under FDA product code LRK (Device, Anti-Snoring). FDA records list one 510(k) clearance for Hays & Meade, Inc. As of , FDA records show no recalls naming K882303.

Clearance record

Decision date
Received
(315 days to decision)
Product code
LRK Device, Anti-Snoring
Regulation
21 CFR 872.5570
Device class
Class II
Review panel
Dental
Applicant
Hays & Meade, Inc. P.O. Box 25565, Albuquerque NM
Third party review
No

Clearances, product code LRK

Trailing 12 months
13 clearances under product code LRK in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code LRK, trailing twelve months
MonthClearances
November 20253
December 20252
January 20260
February 20260
March 20262
April 20261
May 20261
June 20262
July 20261
August 20261
September 20260
October 20260