510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K873300Substantially Equivalent

Service Master (Impulse)

Richards Medical Co., Inc., Memphis TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873300 is the FDA 510(k) clearance record for SERVICE MASTER (IMPULSE), a class I device, cleared for Richards Medical Co., Inc. on under FDA product code LRB (Face Plate Hearing Aid). FDA records list 71 510(k) clearances for Richards Medical Co., Inc., from to . As of , FDA records show no recalls naming K873300.

Clearance record

Decision date
Received
(112 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
Richards Medical Co., Inc. 1450 Brooks Rd., Memphis TN
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