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

Device, Vein Location, Liquid Crystal

21 CFR 880.6970 / General Hospital
FDA source (opens on fda.gov)

KZA is the FDA product code for Device, Vein Location, Liquid Crystal, a class I device type, regulated under 21 CFR 880.6970. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
KZA
Device name
Device, Vein Location, Liquid Crystal
Regulation
21 CFR 880.6970
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
6
Ingested recalls
2

Clearances, product code KZA

By decision year
6 clearances under product code KZA with a decision year between 1978 and 2016, 1978 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code KZA by decision year
YearClearances
19782
19981
20041
20111
20161

Applicants with the most clearances

Product code KZA
Applicants holding the most 510(k) clearances under product code KZA
ApplicantClearances
Harco Products2
Infrared Imaging Systems, Inc.1
Ironmaster, Inc.1
Novarix Limited1
Vuetek Scientific, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 26 companies shown, in name order