SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE— 510(k) K873892

Name: FDA 510(k) clearance K873892
Creator: U.S. Food and Drug Administration
Published: 1988-02-02

Substantially Equivalent

Laserguide

FDA 510(k) clearance K873892 for SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE, Substantially Equivalent on 1988-02-02. Applicant: Laserguide. Device class: 2.

Clearance details

Applicant: Laserguide
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1987-09-23
Decision date: 1988-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Barbara, CA, US

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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 Laserguide

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K880071 — SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE1988-03-22
K875104 — SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE1988-02-02
K873571 — LIGHT-TOUCH FIBEROPTIC MICROCONTACT PROBE1987-11-06
K873664 — LIGHT-SPOT FIBEROPTIC LASER HANDPIECE1987-11-06

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