JLG — Conversion To Ferric Hydroxymates (Colorimetric), Fatty Acids Class I

FDA Device Classification

FDA product code JLG covers "Conversion To Ferric Hydroxymates (Colorimetric), Fatty Acids", a Class I medical device regulated under 21 CFR 862.1290. 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
JLG
Device Class
Class I
Regulation Number
862.1290
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K812081wako chemicals usaWAKO NEFA C TESTAugust 12, 1981
K760750dennison manufacturingSTERILE TUBULAR UNBLEACHED STOCKINETTEOctober 8, 1976