DMR — Solution, M-Nitrophenol, Specific Reagent For Cholinesterase Class I

FDA Device Classification

FDA product code DMR covers "Solution, M-Nitrophenol, Specific Reagent For Cholinesterase", a Class I medical device regulated under 21 CFR 862.3240. Submissions are reviewed by the Clinical Toxicology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
DMR
Device Class
Class I
Regulation Number
862.3240
Submission Type
Review Panel
TX
Medical Specialty
Clinical Toxicology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K790986wampole laboratoriesRF CONTROLSJune 28, 1979