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

Dispenser, Liquid Medication

21 CFR 880.6430 / General Hospital
FDA source (opens on fda.gov)

KYX is the FDA product code for Dispenser, Liquid Medication, a class I device type, regulated under 21 CFR 880.6430. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and 17 recalls.

Classification record

Product code
KYX
Device name
Dispenser, Liquid Medication
Regulation
21 CFR 880.6430
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
11
Ingested recalls
17

Clearances, product code KYX

By decision year
11 clearances under product code KYX with a decision year between 1976 and 2015, 1980 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KYX by decision year
YearClearances
19761
19771
19781
19791
19803
19831
19951
19981
20151

Applicants with the most clearances

Product code KYX
Applicants holding the most 510(k) clearances under product code KYX
ApplicantClearances
Burron Medical Products, Inc.3
Baxa Corp., Sub. of Cook Group, Inc.1
Canyon Medical Products1
Kleengel, LLC1
Landmark Plastics1
National Patent Development Corp.1
Pharmaseal Laboratories1
Sangstat Medical Corp.1
Tridak1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 254 companies shown, in name order