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

Collimator, Dermatological, Therapeutic X-Ray

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

IYL is the FDA product code for Collimator, Dermatological, 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
IYL
Device name
Collimator, Dermatological, 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 IYL

By decision year
1 clearance under product code IYL with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IYL by decision year
YearClearances
19841

Applicants with the most clearances

Product code IYL
Applicants holding the most 510(k) clearances under product code IYL
ApplicantClearances
Treace Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code