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

Irradiator, Blood To Prevent Graft Versus Host Disease

Unknown
FDA source (opens on fda.gov)

MOT is the FDA product code for Irradiator, Blood To Prevent Graft Versus Host Disease. As of , FDA records hold 16 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
MOT
Device name
Irradiator, Blood To Prevent Graft Versus Host Disease
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
16
Ingested recalls
2

Clearances, product code MOT

By decision year
16 clearances under product code MOT with a decision year between 1983 and 2020, 1995 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code MOT by decision year
YearClearances
19831
19851
19871
19953
19961
19981
20031
20052
20091
20161
20171
20191
20201

Applicants with the most clearances

Product code MOT
Applicants holding the most 510(k) clearances under product code MOT
ApplicantClearances
Mds Nordion3
Best Theratronics Ltd.2
J. L. Shepherd and Assoc.2
Nordion International, Inc.2
Atomic Energy of Canada1
Cis-Us, Inc.1
Hitachi, Ltd.1
R3 X-Ray L.L.C1
Rad-Source Technologies, Inc.1
Rad-Source, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code