510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
DMRClass I

Solution, M-Nitrophenol, Specific Reagent For Cholinesterase

21 CFR 862.3240 / Clinical Toxicology
FDA source (opens on fda.gov)

DMR is the FDA product code for Solution, M-Nitrophenol, Specific Reagent For Cholinesterase, a class I device type, regulated under 21 CFR 862.3240. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DMR
Device name
Solution, M-Nitrophenol, Specific Reagent For Cholinesterase
Regulation
21 CFR 862.3240
Device class
Class I
Review panel
Clinical Toxicology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code DMR

By decision year
1 clearance under product code DMR with a decision year between 1979 and 1979, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DMR by decision year
YearClearances
19791

Applicants with the most clearances

Product code DMR
Applicants holding the most 510(k) clearances under product code DMR
ApplicantClearances
Wampole Laboratories1

Companies listing this code with FDA

Companies whose registered establishments list this code

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