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

Disinfectant, Medical Devices

21 CFR 880.6890 / General Hospital
FDA source (opens on fda.gov)

LRJ is the FDA product code for Disinfectant, Medical Devices, a class I device type, regulated under 21 CFR 880.6890. As of , FDA records hold 73 510(k) clearances under this code, the most recent dated , and 17 recalls.

Classification record

Product code
LRJ
Device name
Disinfectant, Medical Devices
Regulation
21 CFR 880.6890
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
73
Ingested recalls
17

Clearances, product code LRJ

By decision year
73 clearances under product code LRJ with a decision year between 1987 and 1999, 1995 the highest year at 28.
Show the numbers
510(k) clearances under FDA product code LRJ by decision year
YearClearances
19872
19891
19924
19931
199410
199528
199615
19972
19987
19993

Applicants with the most clearances

Product code LRJ
Applicants holding the most 510(k) clearances under product code LRJ
ApplicantClearances
Central Solutions, Inc.7
Huntington Laboratories, Inc.6
Calgon Vestal Div.5
Caltech Industries, Inc.5
Sporicidin Intl.5
Convatec, A Division of E.R. Squibb & Sons4
S.C. Johnson & Son, Inc.4
Metrex Research3
National Laboratories3
Alcide Corp.2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 367 companies shown, in name order