JAOClass II

Scanner, Fluorescent

21 CFR 892.1220 / Radiology

JAO is the FDA product code for Scanner, Fluorescent, a class II device type, regulated under 21 CFR 892.1220. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1991-08-20, and no recalls.

Classification record

Product code: JAO
Device name: Scanner, Fluorescent
Regulation: 21 CFR 892.1220
Device class: Class II
Review panel: Radiology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code JAO

By decision year

2 clearances under product code JAO with a decision year between 1990 and 1991, 1990 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code JAO by decision year
Year	Clearances
1990	1
1991	1

Applicants with the most clearances

Product code JAO

Applicants holding the most 510(k) clearances under product code JAO
Applicant	Clearances
Abiomed, Inc.	1
Montifore Medical Center	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code JAO.

Recent clearances

Product code JAO

Recent recalls

Product code JAO

FDA records show no recalls under product code JAO.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)