FLEXIBLE LIQUID LIGHT GUIDE— 510(k) K834487

Substantially Equivalent

Endo Lase, Inc.

FDA 510(k) clearance K834487 for FLEXIBLE LIQUID LIGHT GUIDE, Substantially Equivalent on 1984-02-21. Applicant: Endo Lase, Inc.. Device class: 2.

Clearance details

Applicant: Endo Lase, Inc.
Product code: Code FFS
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1983-12-13
Decision date: 1984-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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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.