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

Dish, Tissue Culture

21 CFR 864.2240 / Hematology
FDA source (opens on fda.gov)

KIZ is the FDA product code for Dish, Tissue Culture, a class I device type, regulated under 21 CFR 864.2240. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KIZ
Device name
Dish, Tissue Culture
Regulation
21 CFR 864.2240
Device class
Class I
Review panel
Hematology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
8
Ingested recalls
0

Clearances, product code KIZ

By decision year
8 clearances under product code KIZ with a decision year between 1979 and 1989, 1979 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code KIZ by decision year
YearClearances
19792
19821
19852
19872
19891

Applicants with the most clearances

Product code KIZ
Applicants holding the most 510(k) clearances under product code KIZ
ApplicantClearances
BD Becton Dickinson Vacutainer Systems Preanalytic1
Corning Medical & Scientific1
Dynatech Corp.1
Dynatech Laboratories, Inc.1
Howmedica Corp.1
Isratech Marketing Corp.1
Lifetrac, Inc.1
Nunc, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 62 companies shown, in name order