510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K942722Substantially Equivalent

Module Program

Electone, Inc., Winter Park FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K942722 is the FDA 510(k) clearance record for MODULE PROGRAM, a class I device, cleared for Electone, Inc. on under FDA product code LRB (Face Plate Hearing Aid). FDA records list 73 510(k) clearances for Electone, Inc., from to . As of , FDA records show no recalls naming K942722.

Clearance record

Decision date
Received
(89 days to decision)
Product code
LRB Face Plate Hearing Aid
Regulation
21 CFR 874.3300
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Electone, Inc. P.O. Box 910, Winter Park FL
510(k) summary
Statement
Third party review
No

Clearances, product code LRB

Trailing 12 months

FDA records hold no clearances under product code LRB in the trailing twelve months.

FDA records show no clearances under product code LRB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LRB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260