inforMED
QUEClass II

Spinal Muscular Atrophy Newborn Screening Test System

Immunology · 21 CFR 866.5980

A Spinal Muscular Atrophy (SMA) newborn screening test system is a prescription device intended to detect homozygous deletion of exon 7 or other similar mutations in the SMN1 (Survival Motor Neuron 1) gene of DNA obtained from dried blood spot specimens on filter paper using a polymerase chain reaction-based test as an aid in screening newborns for SMA. Presumptive positive results are intended to be followed up by diagnostic confirmatory testing.

MDR events0All time
Recalls0All time
Registered firms1Currently listed
510(k) clearances1All time

Recent MDR events

0 adverse event reports on file

See all →

No MDR events on file for this product code.

Event type breakdown

No data available.

Most-reported manufacturers

See all →

No data available.

Recalls

0 recall events for this product code

See all →

No recalls on file for this product code.

Registered firms

1 firms currently registered for this product code

See all →

510(k) clearances

1 clearances for this product code

See all →