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

Generator, Low Voltage, Therapeutic X-Ray

21 CFR 892.5900 / Radiology
FDA source (opens on fda.gov)

IYD is the FDA product code for Generator, Low Voltage, Therapeutic X-Ray, a class II device type, regulated under 21 CFR 892.5900. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
IYD
Device name
Generator, Low Voltage, Therapeutic X-Ray
Regulation
21 CFR 892.5900
Device class
Class II
Review panel
Radiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code IYD

By decision year
1 clearance under product code IYD with a decision year between 1993 and 1993, 1993 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IYD by decision year
YearClearances
19931

Applicants with the most clearances

Product code IYD
Applicants holding the most 510(k) clearances under product code IYD
ApplicantClearances
Toshiba America Medical Systems, In.C1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code IYD.