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

Gas Chromatography, Methadone

21 CFR 862.3620 / Clinical Toxicology
FDA source (opens on fda.gov)

DMB is the FDA product code for Gas Chromatography, Methadone, a class II device type, regulated under 21 CFR 862.3620. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DMB
Device name
Gas Chromatography, Methadone
Regulation
21 CFR 862.3620
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 DMB

By decision year
1 clearance under product code DMB with a decision year between 1991 and 1991, 1991 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DMB by decision year
YearClearances
19911

Applicants with the most clearances

Product code DMB
Applicants holding the most 510(k) clearances under product code DMB
ApplicantClearances
Syva Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code