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DLR — Hemagglutination Inhibition, Morphine Class II

FDA Device Classification

Classification Details

Product Code
DLR
Device Class
Class II
Regulation Number
862.3640
Submission Type
Review Panel
TX
Medical Specialty
Clinical Toxicology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K791551technamHI-M-TEST MORPHINEOctober 17, 1979
K760074j.t. baker chemicalKIT, MORPHINE (TOXI-PAK IMMUNO HI)July 20, 1976