Product code JAO

Device name: Scanner, Fluorescent
Medical specialty: Radiology
Device class: 2
Regulation number: 892.1220
Review panel: RA
Implant: N
Life sustaining/supporting: N
GMP exempt: N
Third party review: Y
Summary malfunction reporting: Eligible
Source: FDA openFDA device classification dataset

510(k), Device, Applicant table
510(k)	Device	Applicant	Decision date
K911749	L-LINEX-RAY FLUORESCENCE	Montifore Medical Center	1991-08-20
K900574	ABIOMED BODY LEAD ANALYZER MODEL 200/20	Abiomed, Inc.	1990-03-15