JLC — Nitroprusside Reaction (Qualitative, Urine), Cystine Class I

FDA Device Classification

FDA product code JLC covers "Nitroprusside Reaction (Qualitative, Urine), Cystine", a Class I medical device regulated under 21 CFR 862.1240. Submissions are reviewed by the Clinical Chemistry panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JLC
Device Class
Class I
Regulation Number
862.1240
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K843382mission pharmacalUROCYSTINJanuary 8, 1985
K810514sandare chemical coSANDARE NITROPRUSSIDE TEST PROCEDUREMarch 4, 1981