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

Assay, T Lymphocyte Surface Marker

21 CFR 864.5220 / Hematology
FDA source (opens on fda.gov)

LIZ is the FDA product code for Assay, T Lymphocyte Surface Marker, a class II device type, regulated under 21 CFR 864.5220. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
LIZ
Device name
Assay, T Lymphocyte Surface Marker
Regulation
21 CFR 864.5220
Device class
Class II
Review panel
Hematology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
7
Ingested recalls
1

Clearances, product code LIZ

By decision year
7 clearances under product code LIZ with a decision year between 1982 and 1992, 1984 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LIZ by decision year
YearClearances
19821
19831
19842
19851
19861
19921

Applicants with the most clearances

Product code LIZ
Applicants holding the most 510(k) clearances under product code LIZ
ApplicantClearances
BD Becton Dickinson Vacutainer Systems Preanalytic2
Bio-Rad1
Control Diagnostics1
Gen Trak, Inc.1
Ortho Diagnostic Systems, Inc.1
Technicon Instruments Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code