510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
IWXClass I

Barrier, Control Panel, X-Ray, Movable

21 CFR 892.6500 / Radiology
FDA source (opens on fda.gov)

IWX is the FDA product code for Barrier, Control Panel, X-Ray, Movable, a class I device type, regulated under 21 CFR 892.6500. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
IWX
Device name
Barrier, Control Panel, X-Ray, Movable
Regulation
21 CFR 892.6500
Device class
Class I
Review panel
Radiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
1

Clearances, product code IWX

By decision year
3 clearances under product code IWX with a decision year between 1978 and 1988, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IWX by decision year
YearClearances
19781
19851
19881

Applicants with the most clearances

Product code IWX
Applicants holding the most 510(k) clearances under product code IWX
ApplicantClearances
A2j, Inc.1
Tecnomed, Inc.1
Victoreen, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 24 companies shown, in name order