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

Fluoroscopic X-Ray Image Intensifier

21 CFR 892.1960 / Radiology
FDA source (opens on fda.gov)

QHX is the FDA product code for Fluoroscopic X-Ray Image Intensifier, a class I device type, regulated under 21 CFR 892.1960. FDA's definition for this code reads: "To instantaneously convert an x-ray pattern from a fluoroscopic x-ray system into a corresponding light image of higher energy density". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
QHX
Device name
Fluoroscopic X-Ray Image Intensifier
FDA definition
To instantaneously convert an x-ray pattern from a fluoroscopic x-ray system into a corresponding light image of higher energy density.
Regulation
21 CFR 892.1960
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
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code

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