MEDILAS 2— 510(k) K853580

Substantially Equivalent

Endo Lase, Inc.

FDA 510(k) clearance K853580 for MEDILAS 2, Substantially Equivalent on 1986-02-13. Applicant: Endo Lase, Inc.. Device class: 3.

Clearance details

Applicant: Endo Lase, Inc.
Product code: Code LKW
Device class: Class 3
Advisory panel: Unknown
Date received: 1985-08-26
Decision date: 1986-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LKW

K875042 — ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY1988-06-24
K880172 — MODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA.1988-03-11
K864166 — 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY1987-02-10
K844440 — MODEL 4000 ND:YAG LASER FOR HEMORRHAGE CONTROL1985-05-09

More clearances from Endo Lase, Inc.

K853900 — ENDO-LASE CD40 FOR NEUROSURGERY1986-06-18
K853878 — ENDO-LASE CD-100 CO2 LASER FOR NEUROSURGERY1986-05-02
K853876 — ENDO-LSE CD-100 CO2 LASER FOR GYNECOLOGY1986-02-21
K853903 — ENDO-LASE CD40 CO2 FOR GYNECOLOGY1986-02-21
K855093 — MEDILAS 2 ND:YAG LASER SURGERY SYSTEM1986-02-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.