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

Media, Reusable Image

21 CFR 892.1840 / Radiology
FDA source (opens on fda.gov)

LQA is the FDA product code for Media, Reusable Image, a class I device type, regulated under 21 CFR 892.1840. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LQA
Device name
Media, Reusable Image
Regulation
21 CFR 892.1840
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
1
Ingested recalls
0

Clearances, product code LQA

By decision year
1 clearance under product code LQA with a decision year between 1986 and 1986, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LQA by decision year
YearClearances
19861

Applicants with the most clearances

Product code LQA
Applicants holding the most 510(k) clearances under product code LQA
ApplicantClearances
Digirad Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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