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

Detectors And Removers, Lice, (Including Combs)

21 CFR 880.5960 / General Hospital
FDA source (opens on fda.gov)

LJL is the FDA product code for Detectors And Removers, Lice, (Including Combs), a class I device type, regulated under 21 CFR 880.5960. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LJL
Device name
Detectors And Removers, Lice, (Including Combs)
Regulation
21 CFR 880.5960
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
11
Ingested recalls
0

Clearances, product code LJL

By decision year
11 clearances under product code LJL with a decision year between 1982 and 2017, 1998 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code LJL by decision year
YearClearances
19822
19941
19983
19991
20092
20172

Applicants with the most clearances

Product code LJL
Applicants holding the most 510(k) clearances under product code LJL
ApplicantClearances
Care Technologies, Inc.2
Larada Sciences Inc.2
Epilady 2000, LLC1
Innomed, Inc.1
Innovative Products, Inc.1
Kiel Laboratories, Inc.1
MedTech Products, Inc.1
National Pediculosis Assoc.1
Piedmont Pharmaceuticals, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 47 companies shown, in name order