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
RDWNot classified

General Purpose Laser Products

Unknown
FDA source (opens on fda.gov)

RDW is the FDA product code for General Purpose Laser Products. FDA's definition for this code reads: "Product, laser, general, emit beam; A laser or product containing a laser that is intended for general purpose use". As of , FDA records hold no 510(k) clearances under this code and 5 recalls.

Classification record

Product code
RDW
Device name
General Purpose Laser Products
FDA definition
Product, laser, general, emit beam; A laser or product containing a laser that is intended for general purpose use.
Device class
Not classified
Review panel
Unknown
Submission type
FDA code null
GMP exempt
Yes
Ingested clearances
0
Ingested recalls
5

Companies listing this code with FDA

Companies whose registered establishments list this code

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