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
LKBUnclassified

Pad, Alcohol, Device Disinfectant

Unknown
FDA source (opens on fda.gov)

LKB is the FDA product code for Pad, Alcohol, Device Disinfectant. As of , FDA records hold 25 510(k) clearances under this code, the most recent dated , and 9 recalls.

Classification record

Product code
LKB
Device name
Pad, Alcohol, Device Disinfectant
Device class
Unclassified
Review panel
Unknown
Submission type
FDA code 7
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
25
Ingested recalls
9

Clearances, product code LKB

By decision year
25 clearances under product code LKB with a decision year between 1981 and 2014, 1983 the highest year at 6.
Show the numbers
510(k) clearances under FDA product code LKB by decision year
YearClearances
19811
19836
19842
19851
19861
19871
19895
19902
19913
20121
20131
20141

Applicants with the most clearances

Product code LKB
Applicants holding the most 510(k) clearances under product code LKB
ApplicantClearances
Aplicare, Inc.4
Concord Laboratories, Inc.3
Span-America Medical Systems, Inc.3
Acme United Corp.1
Bausch & Lomb Incorporated1
Beckman Instruments, Inc.1
Becton Dickinson & Co1
Bowen & Company, Inc.1
Bard Access Systems, Inc.1
Cederroth, Inc. USA1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 100 companies shown, in name order