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JLA — Conversion To Creatinine, Creatine Class I

FDA Device Classification

Classification Details

Product Code
JLA
Device Class
Class I
Regulation Number
862.1210
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K852767panmedERYTHOCYTE CREATINENovember 13, 1986
K854016american bioproductsASSERACHROM PROTEIN C KITJanuary 3, 1986