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

High Pressure Liquid Chromatography, Benzodiazepine

21 CFR 862.3170 / Clinical Toxicology
FDA source (opens on fda.gov)

LAA is the FDA product code for High Pressure Liquid Chromatography, Benzodiazepine, a class II device type, regulated under 21 CFR 862.3170. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LAA
Device name
High Pressure Liquid Chromatography, Benzodiazepine
Regulation
21 CFR 862.3170
Device class
Class II
Review panel
Clinical Toxicology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code LAA

By decision year
1 clearance under product code LAA with a decision year between 1996 and 1996, 1996 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LAA by decision year
YearClearances
19961

Applicants with the most clearances

Product code LAA
Applicants holding the most 510(k) clearances under product code LAA
ApplicantClearances
Bio-Rad1

Companies listing this code with FDA

Companies whose registered establishments list this code

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