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

Test, Temperature Discrimination

21 CFR 882.1200 / Neurology
FDA source (opens on fda.gov)

LQW is the FDA product code for Test, Temperature Discrimination, a class I device type, regulated under 21 CFR 882.1200. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LQW
Device name
Test, Temperature Discrimination
Regulation
21 CFR 882.1200
Device class
Class I
Review panel
Neurology
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
0

Clearances, product code LQW

By decision year
3 clearances under product code LQW with a decision year between 1987 and 2014, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LQW by decision year
YearClearances
19871
19931
20141

Applicants with the most clearances

Product code LQW
Applicants holding the most 510(k) clearances under product code LQW
ApplicantClearances
Medoc Corp.1
Prosenex1
Sensortek, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code