ND: YAGLASER FOR PALLIATIVE TREAT OF OBSTRUCTION— 510(k) K852507

Name: FDA 510(k) clearance K852507
Creator: U.S. Food and Drug Administration
Published: 1985-07-05

Substantially Equivalent

Endo Lase, Inc.

FDA 510(k) clearance K852507 for ND: YAGLASER FOR PALLIATIVE TREAT OF OBSTRUCTION, Substantially Equivalent on 1985-07-05. Applicant: Endo Lase, Inc.. Device class: 2.

Clearance details

Applicant: Endo Lase, Inc.
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1985-06-12
Decision date: 1985-07-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLO

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K884815 — SLT CLMD CONTACT LASER1988-12-22
K881499 — SURGILASE YAG 100 FOR GYNECOLOGY USE1988-04-29
K880592 — LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE1988-04-25
K880170 — MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS1988-03-24
K874254 — ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS1988-03-04

More clearances from Endo Lase, Inc.

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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.