JKJ — Fluorometric Measurement, Porphyrins Class I

FDA Device Classification

FDA product code JKJ covers "Fluorometric Measurement, Porphyrins", a Class I medical device regulated under 21 CFR 862.1595. Submissions are reviewed by the Clinical Chemistry panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JKJ
Device Class
Class I
Regulation Number
862.1595
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K893038helena laboratoriesPROTOFLUOR ZNovember 17, 1989
K871499helena laboratoriesPROTOFLUOR ZAugust 25, 1987
K780455whale scientificQUANTITATIVE DETERMINATION OF PORPHYRINSJuly 27, 1978