ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEM— 510(k) K860063

Name: FDA 510(k) clearance K860063
Creator: U.S. Food and Drug Administration
Published: 1986-02-05

Substantially Equivalent

Laser Media

FDA 510(k) clearance K860063 for ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEM, Substantially Equivalent on 1986-02-05. Applicant: Laser Media. Device class: 2.

Clearance details

Applicant: Laser Media
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1986-01-06
Decision date: 1986-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hauppauge, NY, 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 Laser Media

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K872352 — FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA1987-12-30
K872351 — FIBERLASE II ND:YAG LASER FOR PULMONARY USE1987-12-11
K872350 — FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE1987-08-10
K872031 — UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEM1987-08-04
K863428 — SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAG1986-12-03

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