PQT — Alpha-L-Iduronidase (Idua) Newborn Screening Test System Class II

FDA Device Classification

FDA product code PQT covers "Alpha-L-Iduronidase (Idua) Newborn Screening Test System", a Class II medical device regulated under 21 CFR 862.1488. Submissions are reviewed by the Clinical Chemistry panel.

Classification Details

Product Code
PQT
Device Class
Class II
Regulation Number
862.1488
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Definition

Intended for quantitative measurement of the activity of alpha-L-iduronidase (IDUA) from newborn dried blood spot specimens.