Laser Engineering, Inc.
FDA 510(k) medical device clearances.
Top product codes for Laser Engineering, Inc.
Recent clearances by Laser Engineering, Inc.
- K211605 — Dual Switch
- K141908 — DUAL SWITCH
- K924457 — MICROMANIPULATOR
- K912247 — UNIVERSAL COUPLER, LAPAROSCOPIC ACCESSORY
- K912347 — BIPURE 1000
- K910062 — 02-10,001
- K911852 — COMPULSE CO2 SURGICAL LASER SYS.
- K905676 — MD CO2 SURGICAL LASER SYSTEM/GEN. SURGERY AND ORTH
- K875314 — GL-35 COLPOSCOPIC LASER SYSTEM
- K881580 — MODEL MD-25 CO2 LASER FOR DERMA./PLASTIC SURGERY
- K881581 — MODEL MD-45 CO2 LASER FOR OB-GYN & UROLOGICAL USE
- K881582 — MODEL MD-45 CO2 LASER FOR DERMATOLOGY/PODIATRY USE
- K881583 — MODEL MD-25 CO2 LASER FOR EAR, NOSE & THROAT
- K881584 — MODEL MD-45 CO2 LASER FOR NEUROSURGERY USE
- K881585 — MODEL MD-25 CO2 LASER FOR NEUROSURGERY USE
- K881586 — MODEL MD-45 CO2 LASER FOR ENT APPLICATIONS
- K881587 — MODEL MD-25 CO2 LASER FOR PODIATRY APPLICATIONS
- K881588 — MODEL MD-25 LASER FOR SURGICAL USE
Data sourced from openFDA. This site is unofficial and independent of the FDA.