510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K083206Substantially Equivalent

Lousebuster

Larada Sciences Inc., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K083206 is the FDA 510(k) clearance record for LOUSEBUSTER, a class I device, cleared for Larada Sciences on under FDA product code LJL (Detectors And Removers, Lice, (Including Combs)). FDA records list 2 510(k) clearances for Larada Sciences, from to . As of , FDA records show no recalls naming K083206.

Clearance record

Decision date
Received
(130 days to decision)
Product code
LJL Detectors And Removers, Lice, (Including Combs)
Regulation
21 CFR 880.5960
Device class
Class I
Review panel
General Hospital
Applicant
Larada Sciences 148 S. 1200 E., Salt Lake City UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LJL

Trailing 12 months

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

FDA records show no clearances under product code LJL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LJL, 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