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

Recorder, Attention Task Performance

Unknown
FDA source (opens on fda.gov)

LQD is the FDA product code for Recorder, Attention Task Performance. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LQD
Device name
Recorder, Attention Task Performance
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
11
Ingested recalls
0

Clearances, product code LQD

By decision year
11 clearances under product code LQD with a decision year between 1986 and 2018, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LQD by decision year
YearClearances
19862
19911
20021
20041
20121
20142
20161
20171
20181

Applicants with the most clearances

Product code LQD
Applicants holding the most 510(k) clearances under product code LQD
ApplicantClearances
Qbtech AB4
The Tova Company2
Anthrotronix, Inc.1
Clinical Diagnostics, Inc.1
Infantest Corp.1
Optax Systems, Inc.1
Performance Ent.1

Companies listing this code with FDA

Companies whose registered establishments list this code