Home / Device Classification / JJP

JJP — Electrode, Ion Selective (Non-Specified) Class I

FDA Device Classification

FDA product code JJP covers "Electrode, Ion Selective (Non-Specified)", a Class I medical device regulated under 21 CFR 862.2050. 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
JJP
Device Class
Class I
Regulation Number
862.2050
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K900280amiconCENTRIPREP 100February 16, 1990
K863438nova biomedicalNOVA II SODIUM/POTASSIUM/LITHIUM ANALYZERSeptember 29, 1986
K860143reagent laboratoryURINE DILUENT-FOR USE WITH ION SELECTIVE ELECTRODEFebruary 10, 1986

FDA data resources