GIQ — Hemoglobin S Class II

FDA Device Classification

FDA product code GIQ covers "Hemoglobin S", a Class II medical device regulated under 21 CFR 864.7415. Submissions are reviewed by the Hematology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
GIQ
Device Class
Class II
Regulation Number
864.7415
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K955719medicus technologiesSICKLE-2000August 14, 1996
K942276isolabQUIK-SEP QUANTITATIVE HEMOGLOBIN S ASSAYJanuary 20, 1995
K874429hf scientificHEMOGLOBIN DETERMINATION TEST KIT HGB S-100 & 12February 4, 1988