ND:YAG LASER UROLOGICAL SURGERY— 510(k) K844459

Name: FDA 510(k) clearance K844459
Creator: U.S. Food and Drug Administration
Published: 1985-01-16

Substantially Equivalent

Endo Lase, Inc.

FDA 510(k) clearance K844459 for ND:YAG LASER UROLOGICAL SURGERY, Substantially Equivalent on 1985-01-16. Applicant: Endo Lase, Inc.. Device class: 2.

Clearance details

Applicant: Endo Lase, Inc.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1984-11-15
Decision date: 1985-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LNK

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K925395 — TECHNOMED PULSOLITH 4000 LASER SYSTEM1993-05-21
K901723 — MDL-2000 LASERTRIPTER1990-07-13
K874253 — ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.1988-07-12
K874255 — ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.1988-07-12
K880193 — MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USE1988-04-14

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.