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

Enzyme Immunoassay, Methotrexate

Unknown
FDA source (opens on fda.gov)

LAO is the FDA product code for Enzyme Immunoassay, Methotrexate. As of , FDA records hold 10 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
LAO
Device name
Enzyme Immunoassay, Methotrexate
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
10
Ingested recalls
2

Clearances, product code LAO

By decision year
10 clearances under product code LAO with a decision year between 1978 and 2024, 1983 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LAO by decision year
YearClearances
19781
19811
19832
19891
19931
20111
20171
20231
20241

Applicants with the most clearances

Product code LAO
Applicants holding the most 510(k) clearances under product code LAO
ApplicantClearances
Ark Diagnostics Inc3
Abbott Medical2
Syva Co.2
Siemens Healthcare Diagnostics Inc.1
E.I. Dupont de Nemours & Co., Inc.1
Roche Diagnostics GmbH1

Companies listing this code with FDA

Companies whose registered establishments list this code