510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
REANot classified

High-Power Laser Light Show Projector

Unknown
FDA source (opens on fda.gov)

REA is the FDA product code for High-Power Laser Light Show Projector. FDA's definition for this code reads: "Product, laser, demo, projector, laser light show/display, class iiib/iv/3b/4; Laser projection system that incorporates a laser having a maximum radiation output power greater than 5mw". As of , FDA records hold no 510(k) clearances under this code and 12 recalls.

Classification record

Product code
REA
Device name
High-Power Laser Light Show Projector
FDA definition
Product, laser, demo, projector, laser light show/display, class iiib/iv/3b/4; Laser projection system that incorporates a laser having a maximum radiation output power greater than 5mw.
Device class
Not classified
Review panel
Unknown
Submission type
FDA code null
GMP exempt
Yes
Ingested clearances
0
Ingested recalls
12

Companies listing this code with FDA

Companies whose registered establishments list this code

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