510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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LZSClass III

Excimer Laser System

Unknown
FDA source (opens on fda.gov)

LZS is the FDA product code for Excimer Laser System, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 29 recalls.

Classification record

Product code
LZS
Device name
Excimer Laser System
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
29

Companies listing this code with FDA

Companies whose registered establishments list this code