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

Device, Antimicrobial Drug Removal

21 CFR 866.2560 / Microbiology
FDA source (opens on fda.gov)

LJF is the FDA product code for Device, Antimicrobial Drug Removal, a class I device type, regulated under 21 CFR 866.2560. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LJF
Device name
Device, Antimicrobial Drug Removal
Regulation
21 CFR 866.2560
Device class
Class I
Review panel
Microbiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code LJF

By decision year
4 clearances under product code LJF with a decision year between 1982 and 2000, 1983 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LJF by decision year
YearClearances
19821
19832
20001

Applicants with the most clearances

Product code LJF
Applicants holding the most 510(k) clearances under product code LJF
ApplicantClearances
Marion Laboratories, Inc.2
BD Becton Dickinson Vacutainer Systems Preanalytic1
bioMerieux, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LJF.